Geneva USA - Jobs

Study Coordinator - San Diego, CA 92152 - San Diego, CA

DESCRIPTION Looking for an exciting new career? Join our team! The Geneva Foundation is a non-profit organization which promotes and supports military medicine. The Foundation has built relationships with highly skilled, exceptionally motivated, world-recognized researchers and medical professionals and hires top-quality staff. By joining The Geneva Foundation, you will have an exciting and stimulating career in which you will advance, "The Future of Military Medicine. Today." The Geneva Foundation is seeking a Study Coordinator to support the Deployment Health Research department's mission conductingepidemiological studies to investigate the longitudinal health outcomes of military personnel, and the impact of military experiences including deployments. Research includes studies of symptoms, hospitalizations, reproductive outcomes, mortality, and other health outcomes among DoD beneficiary populations, both military and civilian. Included among the core programs are the Millennium Cohort Study, Millennium Cohort Family Study, the Birth and Infant Health Registry, and the Recruit Assessment Program, as well as other deployment related studies within the department. This acquisition will provide research support services for conducting epidemiological studies to investigate the longitudinal health outcomes of military personnel, and the impact of military experiences including deployments, vaccinations, and other military experiences. Activities (Tasks) to accomplish this task order involve the following: *Task 1: DoD Healthcare Utilization Data Augment the evaluation and analysis of Department of Defense healthcare utilization data among military, veteran, and dependent populations. The contractor shall clean and edit the increasingly large and complex databases through summarization, mathematical modeling, and interpretation, utilizing complex algorithms and computer programs *Task 2: DoD Healthcare Utilization Data (Exposure and Disease Specific) augment the evaluation and analysis Department of Defense healthcare utilization data among military, veteran, and dependent populations from current military Operations and related deployment health with exposure&8208;specific and disease&8208;specific analyses. Prepare and publish results of the research conducted through technical reports for military use and/or peer reviewed journals for use by the appropriate medical community, as well as present research findings at scientific and military meetings during this performance period. *Task 3: Health Surveillance of Marines augment the evaluation and analysis of results from the baseline health data of more than 10,000 Marines undergoing recruit training in San Diego on an annual basis, and maintain complete health surveillance data on these Marines. Collect and analyze additional questionnaire&8208;based follow&8208;up data, using standardized scannable, self&8208;completed, paper&8208;and pencil health questionnaires. *Task 4: Millenium Cohort Study Support the Millennium Cohort study operations by continuing to follow US military personnel prospectively by using postal surveys and web&8208;based/internet surveys. Establish, maintain, and manage an interactive website with state&8208;of&8208;the&8208;art security features. Conduct very large mailings that include introductory and reminder postcards, Memorial and Veterans Day postcards, and questionnaire packets. Maintain and update web servers which enable mailing surveys and other study materials to 150,000 participants. Securely maintain email addresses for study subjects, and use these email addresses to send invitational emails, Memorial and Veterans Day emails, along with other study relevant electronic communications. Employ consultants as needed to successfully accomplish the work of this study. Cost&8208;saving initiatives (caps, gift cards, and coins) shall be provided to participants as deemed appropriate for the efficient scientific conduction of the study. Follow cohort members previously surveyed, and continue to recruit participation from a new panel of cohort members. Shall design and maintain the survey instruments, and continue to gather self&8208;reported data on demographic characteristics, medical conditions and symptoms, alcohol and smoking behaviors, diet and exercise, as well as new information on deployment&8208;related exposures. Utilize standardized, validated instruments to capture self&8208;assessed physical and mental well&8208;being (SF&8208;36V), mental health diagnoses (Patient Health Questionnaire), and posttraumatic stress disorder (PCL&8208;17). Shall use established cost&8208;effective initiatives to encourage participant website use - these include, but are not limited to, caps, coins, and gift cards. Establish methods to design, produce, mail, and track participant receipt of such initiatives. Develop strategies to maintain participant retention in the study including newsletter as well as other mailers. Clean and analyze the data using complex algorithms and computer programs. Provide periodic assessments of scientific data. *Task 5: DoD Birth and Infant Health Registry collect and analyze data from infants born to military beneficiaries that have been captured in the Department of Defense Birth and Infant Health Registry. The Registry includes data on associated medical conditions, geographic location, and demographics of the military sponsor. Birth defects and other critical health outcomes are identified by International Classification of Diseases, Version 9 (ICD9) coding of inpatient and outpatient encounters. When linked to other standard military databases, important information can be captured on vaccination, occupational, and environmental exposures that may be associated with birth defects. Collaborate with leading experts on this project on exposure&8208;specific and diagnosis&8208;specific analyses. *Task 6: Vaccinations Impact study the impact of vaccinations received among military beneficiaries and specific health outcomes. This work includes creating and working with large military databases. Being facile with their creation and analyses, including date interpretation and writing. *Task 7: Other Research Protocols support other research protocols on deployment and military health within the department by assisting with the execution of these studies from design to completion. DUTIES The Study Coordinator will be responsible for the following: * Perform ICD9 coding of patient encounters * Keep contact data for survey studies * Design and maintain surveys, newsletters, mailers, and other materials * Contact study enrollees by phone, mail, or email * Maintain health surveillance data * Gather self-reported data via questionnaires and standardized forms * Execute research protocols from design to completion QUALIFICATIONS * Bachelors, Masters or PhD Degree in a related field. * Study Coordinators should have experience in one or more of the following disciplines: chemistry, biology, mathematics, botany and geology.

Senior Research Associate - San Diego, CA

DESCRIPTION Looking for an exciting new career? Join our team! The Geneva Foundation is a non-profit organization which promotes and supports military medicine. The Foundation has built relationships with highly skilled, exceptionally motivated, world-recognized researchers and medical professionals and hires top-quality staff. By joining The Geneva Foundation, you will have an exciting and stimulating career in which you will advance, "The Future of Military Medicine. Today." The Geneva Foundation is seeking a Senior Research Associate to support the Deployment Health Research department's mission conducting epidemiological studies to investigate the longitudinal health outcomes of military personnel, and the impact of military experiences including deployments. Research includes studies of symptoms, hospitalizations, reproductive outcomes, mortality, and other health outcomes among DoD beneficiary populations, both military and civilian. Included among the core programs are the Millennium Cohort Study, Millennium Cohort Family Study, the Birth and Infant Health Registry, and the Recruit Assessment Program, as well as other deployment related studies within the department. This acquisition will provide research support services for conducting epidemiological studies to investigate the longitudinal health outcomes of military personnel, and the impact of military experiences including deployments, vaccinations, and other military experiences. Activities (Tasks) to accomplish this task order involve the following: *Task 1: DoD Healthcare Utilization Data Augment the evaluation and analysis of Department of Defense healthcare utilization data among military, veteran, and dependent populations. The contractor shall clean and edit the increasingly large and complex databases through summarization, mathematical modeling, and interpretation, utilizing complex algorithms and computer programs *Task 2: DoD Healthcare Utilization Data (Exposure and Disease Specific) augment the evaluation and analysis Department of Defense healthcare utilization data among military, veteran, and dependent populations from current military Operations and related deployment health with exposure&8208;specific and disease&8208;specific analyses. Prepare and publish results of the research conducted through technical reports for military use and/or peer reviewed journals for use by the appropriate medical community, as well as present research findings at scientific and military meetings during this performance period. *Task 3: Health Surveillance of Marines augment the evaluation and analysis of results from the baseline health data of more than 10,000 Marines undergoing recruit training in San Diego on an annual basis, and maintain complete health surveillance data on these Marines. Collect and analyze additional questionnaire&8208;based follow&8208;up data, using standardized scannable, self&8208;completed, paper&8208;and pencil health questionnaires. *Task 4: Millenium Cohort Study Support the Millennium Cohort study operations by continuing to follow US military personnel prospectively by using postal surveys and web&8208;based/internet surveys. Establish, maintain, and manage an interactive website with state&8208;of&8208;the&8208;art security features. Conduct very large mailings that include introductory and reminder postcards, Memorial and Veterans Day postcards, and questionnaire packets. Maintain and update web servers which enable mailing surveys and other study materials to 150,000 participants. Securely maintain email addresses for study subjects, and use these email addresses to send invitational emails, Memorial and Veterans Day emails, along with other study relevant electronic communications. Employ consultants as needed to successfully accomplish the work of this study. Cost&8208;saving initiatives (caps, gift cards, and coins) shall be provided to participants as deemed appropriate for the efficient scientific conduction of the study. Follow cohort members previously surveyed, and continue to recruit participation from a new panel of cohort members. Shall design and maintain the survey instruments, and continue to gather self&8208;reported data on demographic characteristics, medical conditions and symptoms, alcohol and smoking behaviors, diet and exercise, as well as new information on deployment&8208;related exposures. Utilize standardized, validated instruments to capture self&8208;assessed physical and mental well&8208;being (SF&8208;36V), mental health diagnoses (Patient Health Questionnaire), and posttraumatic stress disorder (PCL&8208;17). Shall use established cost&8208;effective initiatives to encourage participant website use - these include, but are not limited to, caps, coins, and gift cards. Establish methods to design, produce, mail, and track participant receipt of such initiatives. Develop strategies to maintain participant retention in the study including newsletter as well as other mailers. Clean and analyze the data using complex algorithms and computer programs. Provide periodic assessments of scientific data. *Task 5: DoD Birth and Infant Health Registry collect and analyze data from infants born to military beneficiaries that have been captured in the Department of Defense Birth and Infant Health Registry. The Registry includes data on associated medical conditions, geographic location, and demographics of the military sponsor. Birth defects and other critical health outcomes are identified by International Classification of Diseases, Version 9 (ICD9) coding of inpatient and outpatient encounters. When linked to other standard military databases, important information can be captured on vaccination, occupational, and environmental exposures that may be associated with birth defects. Collaborate with leading experts on this project on exposure&8208;specific and diagnosis&8208;specific analyses. *Task 6: Vaccinations Impact study the impact of vaccinations received among military beneficiaries and specific health outcomes. This work includes creating and working with large military databases. Being facile with their creation and analyses, including date interpretation and writing. *Task 7: Other Research Protocols support other research protocols on deployment and military health within the department by assisting with the execution of these studies from design to completion. DUTIES The Senior Research Associate shall be responsible for the following activities: *Clean, edit, and analyze data using complex algorithms and programs * Collect and maintain contact data for survey studies * Prepare and publish results * Design and maintain surveys, newsletters, mailers, and other materials * Contact study enrollees by phone, mail, or email * Monitor and evaluate health surveillance data * Collect and maintain self-reported data via questionnaires and standardized forms * Perform statistical analyses including longitudinal modeling * Analyze adverse/protective effects and health outcomes * Execute research protocols from design to completion QUALIFICATIONS * Masters or PhD Degree in a related field. * Senior Research Associates' should have experience in one or more of the following disciplines: chemistry, biology, mathematics, botany and geology.

Research Assistant - San Diego, CA

DESCRIPTION Looking for an exciting new career? Join our team! The Geneva Foundation is a non-profit organization which promotes and supports military medicine. The Foundation has built relationships with highly skilled, exceptionally motivated, world-recognized researchers and medical professionals and hires top-quality staff. By joining The Geneva Foundation, you will have an exciting and stimulating career in which you will advance, "The Future of Military Medicine. Today." The Geneva Foundation is seeking a Research Assistant to support the Deployment Health Research department's mission conducting epidemiological studies to investigate the longitudinal health outcomes of military personnel, and the impact of military experiences including deployments. Research includes studies of symptoms, hospitalizations, reproductive outcomes, mortality, and other health outcomes among DoD beneficiary populations, both military and civilian. Included among the core programs are the Millennium Cohort Study, Millennium Cohort Family Study, the Birth and Infant Health Registry, and the Recruit Assessment Program, as well as other deployment related studies within the department. This acquisition will provide research support services for conducting epidemiological studies to investigate the longitudinal health outcomes of military personnel, and the impact of military experiences including deployments, vaccinations, and other military experiences. Activities (Tasks) to accomplish this task order involve the following: *Task 1: DoD Healthcare Utilization Data Augment the evaluation and analysis of Department of Defense healthcare utilization data among military, veteran, and dependent populations. The contractor shall clean and edit the increasingly large and complex databases through summarization, mathematical modeling, and interpretation, utilizing complex algorithms and computer programs *Task 2: DoD Healthcare Utilization Data (Exposure and Disease Specific) augment the evaluation and analysis Department of Defense healthcare utilization data among military, veteran, and dependent populations from current military Operations and related deployment health with exposure&8208;specific and disease&8208;specific analyses. Prepare and publish results of the research conducted through technical reports for military use and/or peer reviewed journals for use by the appropriate medical community, as well as present research findings at scientific and military meetings during this performance period. *Task 3: Health Surveillance of Marines augment the evaluation and analysis of results from the baseline health data of more than 10,000 Marines undergoing recruit training in San Diego on an annual basis, and maintain complete health surveillance data on these Marines. Collect and analyze additional questionnaire&8208;based follow&8208;up data, using standardized scannable, self&8208;completed, paper&8208;and pencil health questionnaires. *Task 4: Millenium Cohort Study Support the Millennium Cohort study operations by continuing to follow US military personnel prospectively by using postal surveys and web&8208;based/internet surveys. Establish, maintain, and manage an interactive website with state&8208;of&8208;the&8208;art security features. Conduct very large mailings that include introductory and reminder postcards, Memorial and Veterans Day postcards, and questionnaire packets. Maintain and update web servers which enable mailing surveys and other study materials to 150,000 participants. Securely maintain email addresses for study subjects, and use these email addresses to send invitational emails, Memorial and Veterans Day emails, along with other study relevant electronic communications. Employ consultants as needed to successfully accomplish the work of this study. Cost&8208;saving initiatives (caps, gift cards, and coins) shall be provided to participants as deemed appropriate for the efficient scientific conduction of the study. Follow cohort members previously surveyed, and continue to recruit participation from a new panel of cohort members. Shall design and maintain the survey instruments, and continue to gather self&8208;reported data on demographic characteristics, medical conditions and symptoms, alcohol and smoking behaviors, diet and exercise, as well as new information on deployment&8208;related exposures. Utilize standardized, validated instruments to capture self&8208;assessed physical and mental well&8208;being (SF&8208;36V), mental health diagnoses (Patient Health Questionnaire), and posttraumatic stress disorder (PCL&8208;17). Shall use established cost&8208;effective initiatives to encourage participant website use - these include, but are not limited to, caps, coins, and gift cards. Establish methods to design, produce, mail, and track participant receipt of such initiatives. Develop strategies to maintain participant retention in the study including newsletter as well as other mailers. Clean and analyze the data using complex algorithms and computer programs. Provide periodic assessments of scientific data. *Task 5: DoD Birth and Infant Health Registry collect and analyze data from infants born to military beneficiaries that have been captured in the Department of Defense Birth and Infant Health Registry. The Registry includes data on associated medical conditions, geographic location, and demographics of the military sponsor. Birth defects and other critical health outcomes are identified by International Classification of Diseases, Version 9 (ICD9) coding of inpatient and outpatient encounters. When linked to other standard military databases, important information can be captured on vaccination, occupational, and environmental exposures that may be associated with birth defects. Collaborate with leading experts on this project on exposure&8208;specific and diagnosis&8208;specific analyses. *Task 6: Vaccinations Impact study the impact of vaccinations received among military beneficiaries and specific health outcomes. This work includes creating and working with large military databases. Being facile with their creation and analyses, including date interpretation and writing. *Task 7: Other Research Protocols support other research protocols on deployment and military health within the department by assisting with the execution of these studies from design to completion. DUTIES The Research Assistant shall be responsible for the following: * Perform ICD-9 coding of patient encounters. * Collect and maintain contact data for survey studies * Increase communication between stakeholders (internal and external) by designing and maintaining surveys, newsletters, mailers, and other materials * Initiate communication with study enrollees by phone, mail and/or email * Collect and maintain health surveillance data * Compile self-reported data via questionnaires and standardized forms * Track and execute research protocols from design to completion QUALIFICATIONS REQUIREMENTS: * Bachelors, Masters or PhD Degree in a related field. * Research Assistants' should have experience in one or more of the following disciplines: chemistry, biology, mathematics, botany and geology. * Must have previous experience with ICD-9 coding of patient encounters.

Accounting Manager - Tacoma, WA

Clinical Psychologist - Washington, D.C., DC

DESCRIPTION Looking for an exciting new career? Join our team! The Geneva Foundation is a non-profit organization which promotes and supports military medicine. The Foundation has built relationships with highly skilled, exceptionally motivated, world-recognized researchers and medical professionals and hires top-quality staff. By joining The Geneva Foundation, you will have an exciting and stimulating career in which you will advance, "The Future of Military Medicine. Today." The Clinical Psychologist will provide services that span (and expand) the missions of both the Behavioral Biology Branch and the Military Psychiatry Branch (WRAIR) research programs. The work will be performed primarily in the Washington D.C. metropolitan region, specifically at Walter Reed Army Institute of Research (WRAIR); however some travel (CONUS and OCONUS) will be required in conducting research protocols with Soldiers and units. The Clinical Psychologist shall, with only broad guidance from department and/or center leadership (i.e., with the level of independence that would be expected of an associate research professor at an academic institution), help ensure integrative research between branches in the Center for Military Psychiatry and Neurosciences. This Clinical Psychologist will advise the Center leadership in the development of research efforts that foster inter-branch collaborations. As such, the Clinical Psychologist will be in an advisory and collaborative role as a Center-level asset. In addition, this Clinical Psychologist shall prepare and obtain approvals for mission-relevant human scientific protocols to investigate the interrelationships between sleep parameters, PTSD, personality, combat stress, psychological resilience, psychological distress, physical pain, mTBI, and other militarily relevant factors. The Clinical Psychologist shall collect and analyze data, and present preliminary findings at military, national, and international scientific conferences. The Clinical Research Psychologists shall also serve as author or coauthor on manuscripts resulting from human research protocols. The Clinical Psychologist shall take an active role in mentoring junior-level researchers on Center projects. The Clinical Psychologist shall assist other researchers in the Behavioral Biology Branch and the Military Psychiatry Branch (WRAIR) involved in a wide variety of RAD III-related scientific investigations through discussion, site visits, and collaborative efforts; and participates in department and research team meetings and conferences. DUTIES The Clinical Psychologist shall be capable of performing the following tasks: * Assist Center leadership in developing integrative research protocols spanning multiple Center branches. * Advise the Center Director and Branch Chiefs in the management, supervision, and execution of Center research protocols, particularly ones involving cross-branch collaborations. * Provide scientific expertise in sleep, pain, psychological stress, resilience, PTSD, mTBI, personality, actigraphy, cognitive performance testing, personality testing, neurophysiology, statistical packages. * Perform human research studies (field and laboratory) to include writing protocols, executing protocols, analyzing data, presenting findings up the chain of command, writing final reports, and publishing manuscripts in leading peer-reviewed scientific journals. * Travel as part of duties to locations inside and possibly outside of continental United States. *Travel will be for purposes of developing collaborations, executing research protocols, providing consultative services, and participating in scientific meetings/symposia, etc. * Perform literature searches and literature reviews as part of protocol development and manuscript writing process. Must be comfortable with written English and capable of writing in scientific prose. Especially important in this job will be writing and submitting for publication of scientific research in leading peer-reviewed journals * Perform standard and advanced statistics, using computer-based programs such as SAS, BMDP, etc. Must be proficient with standard Microsoft programs such as Excel, Word, Access, and PowerPoint. * Must be able to work independently and with minimal supervision. Must also be able to function effectively as a member of an interdisciplinary team composed of researchers from a variety of backgrounds/branches/institutions including WRAIR, MRMC, NIH, various universities, etc. * Must be able to train, lead, and/or coordinate technical staff members in all areas of polysomnography, performance testing, and survey development/administration, and additional functions to include (but not limited to) PC-based programming of experimental equipment. * Design graphics for display of study designs, signals, processed data, etc. as necessary for manuscripts for publication in leading refereed journals, poster presentations, technical publications, instructional manuals, field manuals, etc. Other responsibilities include: * Lead support of Center leadership in developing cross-branch research protocols * Must have knowledge, skills, and abilities in multiple Center research domains * Must have ability to guide and execute Center research * Must have knowledge and skills to advise Center Director and Branch Chiefs on all aspects of Center research. *Will be expected to manage/Coordinate Human Studies on a variety of combat-relevant stressors, which will require: * Must have knowledge and skills in pain physiology, neuroanatomy, psychology and sleep deprivation research. * Must have knowledge of and ability to lead, Subject selection/screening, including administration of standardized psychological evaluations. * Must possess knowledge and skills necessary to train and oversee research assistants responsible for executing tasks required by research protocols, including but not limited to ANAM, the psychomotor vigilance task (PVT), and the MWT/MSLT. * Must possess knowledge and ability to personally perform any tasks necessary for an experiment including those mentioned above, initializing and downloading actigraphs and other data, scoring polysomnographic variables for sleep, and other skills as needed for specific studies. Statistical Analysis of Research Data * Knowledge and ability to collect, process, and prepare data for computer entry. * Knowledge and ability to create computer database files for the purpose of analyses and archiving. * Knowledge of, and skills/ability in, statistics and statistical packages for the purpose of data analyses and database management. Prepare Abstracts and Presentations * Must possess knowledge of psychology, stress, pain, and physiology necessary to understand and develop appropriate research objectives. * Must have ability to formulate and organize ideas in order to design scholarly manuscripts. * Must have knowledge of and skills in presentation techniques including design, construction, and actual presentation (i.e., public speaking) skills. * Collaborate With Others in the Creation of Papers for the Purpose of Publication * Must have knowledge, skills, and abilities to mentor and guide junior researchers and technical staff throughout the scientific process from hypothesis generation to publication. * Must Assist all research staff in the development of products whether technical reports or peer-reviewed publications. * Must have knowledge and ability to incorporate computer generated displays into a written document. * Must have knowledge and understanding of relevant databases and accompanying analyses. Contribute to Program Development/Strategic Planning for Center, requiring: * Must possess knowledge, skills, and abilities to help the Director and Branch Chiefs guide strategic program objectives in the Center and branches * Must have a thorough understanding of/familiarity with scientific literature in stress, sleep, PTSD, mTBI, and pain * Program evaluation skills QUALIFICATIONS * PhD or PsyD in Clinical Psychology (APA accredited program), required * Completion of a APA accredited pre-doctoral internship program * 3 years of clinical research experience in lab-based and/or field settings. * The Clinical Psychologist must have at least 20 publications in the peer-reviewed literature demonstrating scientific merit of work and expertise as a research clinical psychologist. * Licensed Clinical Psychologist or the ability to be licensed, required * Clinical or general research experience preferred

Clinical Research Coordinator/Sleep Research Lab Manager - Washington D.C., DC

DESCRIPTION Looking for an exciting new career? Join our team! The Geneva Foundation is a non-profit organization which promotes and supports military medicine. The Foundation has built relationships with highly skilled, exceptionally motivated, world-recognized researchers and medical professionals and hires top-quality staff. By joining The Geneva Foundation, you will have an exciting and stimulating career in which you will advance, "The Future of Military Medicine. Today." This position requires the capability and skills to perform all of the tasks listed for the Sleep/Performance Study coordinators plus extensive knowledge of/experience with FDA regulations, rules, and policies affecting the conduction, record-keeping, and monitoring of human protocols involving investigational new drugs. This position also requires the ability to teach these practices to others (student contractors, enlisted soldiers, etc.) as appropriate, and to monitor study data collection procedures to ensure uniformly high levels of compliance with FDA-required practices throughout all phases of the study: preparation, conduction, analysis, and archiving of clinical data. The study manager also oversees technical and logistical aspects of the conduction of human research in the fields of: sleep, sleep deprivation, electroencephalography, psychophysiology, and others-and aids in the statistical analyses, presentation, and publication of resulting data sets - to include assisting in the preparation of any progress and/or final reports to the FDA and/or commercial (e.g., pharmaceutical industry) sponsors of IND research. Thus, knowledge of ICH/GCP and FDA/CFR guidelines for pharmacological agents used in human use research is a critical requirement. In addition, the Clinical Research Coordinator / Sleep Research Laboratory Manager must become familiar with the USAMRMC MeRITS (Medical Research Information Technology System) for centralized clinical data management, and serve as the Department of Behavioral Biology POC for implementing the various components of this system as they become available. DUTIES ESSENTIAL JOB DUTIES: 1.Oversee/manage technical staff in the conduction of new protocols investigating effects of sleep, sleep loss and pharmacological agents, including investigational new drugs, on cognitive/physiological performance, physiology, efficacy and safety. 2.Study schedule management-i.e., develop and maintain the schedule for use of the sleep laboratory facilities so as to optimize efficient conduction of multiple concurrent studies, taking into consideration the study priorities provided by the Chief of the Department of Behavioral Biology, WRAIR, and the optimal use of both human and material resources required to conduct these studies. 3.Oversee recruitment and screening of volunteers for human research protocols. Ensure that all such records are maintained in a manner that is compliant with FDA rules, regulations, and polices, for those studies involving investigational new drugs. 4.Oversee all aspects of study preparation to include calibration of equipment, ensuring that adequate supplies are on hand for study sessions (e.g., subject food, electrodes, paper/pencil tests, etc.). 5.Develops and maintains SOPs for, and ensures that, all study data are collected, recorded, documented, and eventually archived in a manner consistent with current Good Clinical Practices and any other FDA/government rules and regulations. 6.Perform/oversee monitoring of psychophysiological/physiological equipment as data are recorded on-line. 7.Perform/oversee scoring of sleep stages (including assessment of inter-scorer reliability), compilation of resultant sleep data, and aid in statistical analyses, presentation, and publication of data. 8.Oversee administration and scoring of psychological and performance measures as specified in protocols. 9.Oversee collection of physiological data (e.g., metabolic rate, vital signs) and aid in their analyses and presentation. 10.Assist in the preparation of any progress- and/or final reports submitted to the FDA or commercial entities who are serving as the sponsors of IND research. 11.Perform statistical analyses of data using mainframe and/or PC-based statistical packages under supervision of COR. 12.Develop SOPs and ensure quality control of a variety of laboratory procedures and reviews for the accuracy of test results. Also ensure compliance with pertinent FDA regulations, rules, and policies regarding the processing (collection, recording, storage, and archiving) of all IND study-related data. 13.Serve as head technical resource to the Department of Behavioral Biology, WRAIR, to include training other members of the research team on study-related technical skills, FDA rules, regulations, and policies pertaining to IND studies. 14.Conduct periodic checks of IND data to ensure compliance with all FDA rules, regulations, and policies. Directly assist PIs in dealings with external study monitors and/or FDA inspectors on compliance-related matters/questions regarding data collection, storage, and archiving, as applicable. 15. Become familiar with, and implement, the USAMRMC MeRITS for FDA-compliant clinical data management of IND studies, as this system becomes available. 16. Other duties as assigned. NONESSENTIAL JOB DUTIES: 17.Evaluates and reports on performance of technical staff. 18.Oversees inventory control of laboratory supplies. 19.All other duties as assigned. QUALIFICATIONS Minimum Experience: 2 years in sleep research setting actively involved in protocol execution. Required Knowledge, Skills, and Abilities: High proficiency and experience in the conduction of human studies of investigational new drugs, human research on sleep deprivation and fatigue countermeasures, proficiency with most Windows programs (e.g., Word, Excel, Powerpoint); proficiency on at least 1 mainframe and/or PC-based statistical package; proficiency in the scoring of sleep/wake stages (within 85% agreement of an ABSM diplomate); ability to oversee multiple tasks simultaneously; excellent leadership skills to include ability to develop/maintain excellent professional rapport with research volunteers, research assistants, and other staff members-and the ability to interact effectively with external monitors/inspectors on IND studies. Minimum Education/Training Requirements: *Master's degree in Experimental Psychology or other related field. *Certification as a Clinical Research Coordinator by the Association of Clinical Research Professionals required. *CPR (BLS) certification required Physical Capabilities: Ability to attach psychophysiological equipment (small electrodes, etc) requiring manual dexterity; ability to see small print on a computer monitor; ability to speak clearly; ability to hear. Light lifting and moving of equipment may be required. Must be capable of moving about and standing for long periods of time during study work shifts.

Researcher (Scientific) - Washington D.C., DC

DESCRIPTION Looking for an exciting new career? Join our team! The Geneva Foundation is a non-profit organization which promotes and supports military medicine. The Foundation has built relationships with highly skilled, exceptionally motivated, world-recognized researchers and medical professionals and hires top-quality staff. By joining The Geneva Foundation, you will have an exciting and stimulating career in which you will advance, "The Future of Military Medicine. Today." The Researcher is to provide services for the Department of Behavioral Biology, WRAIR, Research Program. The work will be performed primarily in the Washington D.C. metropolitan region, specifically at Walter Reed Army Institute of Research (WRAIR). The Researcher must be able to lead a multidisciplinary team of doctoral level scientific researchers, to include physicians, psychologists, physiologists and statisticians. The Researcher must be able to critically analyze and review multidisciplinary research proposals and publications for military relevance and scientific adequacy. The Researcher shall prepare and obtain approvals for human scientific protocols to investigate the relationships between sleep parameters and cognitive performance, alertness, personality, and militarily relevant disorders (e.g., PTSD, mTBI) - in accordance with department mission requirements and in support of the recently reorganized Physiological Health Program Area and the Psychological Health Program Area of the Military Operational Medicine Research Area Directorate (RAD III). The Researcher shall collect and analyze data and present preliminary findings at military, national, and international scientific conferences (OCONUS and/or CONUS travel may be required). Researcher shall also serve as author or coauthor on manuscripts resulting from these data collection efforts. The Researcher shall assist other researchers in the Department of Behavioral Biology, WRAIR, involved in RAD III-related scientific investigations through discussion, site visits, and collaborative efforts and participate in department and research team meetings and conferences. DUTIES The Researcher shall be capable of performing the following tasks: * Provide scientific expertise in psychophysiology, actigraphy, cognitive performance testing, personality testing, neurophysiology, statistical packages and functional brain imaging. Perform human research studies (field and laboratory) to include writing protocols, executing protocols, analyzing data, and writing manuscripts. * Travel as part of duties to locations inside and possibly outside of continental United States. Travel will be for purposes of developing collaborations, executing research, and participating in scientific meetings/symposia, etc. * Perform literature searches and literature reviews as part of protocol development and manuscript writing process. Must be comfortable with written English and capable of writing in scientific prose. Important in this job will be writing and submitting for publication scientific research. * Perform standard and advanced statistics, using computer-based programs such as SPSS, BMDP, etc. Must be familiar with standard Microsoft programs such as Excel, Word, Access, and PowerPoint. * Must be able to work independently and with minimal supervision. Must also be able to function effectively as a leader of an interdisciplinary team composed of researchers from a variety of backgrounds/institutions including WRAIR, MRMC, NIH, various universities, etc. * Provide technical support in actigraph utilization for all research studies (field and laboratory) to include maintenance, testing, trouble-shooting, and repair of actigraphs. * Must be able to train, lead, and/or coordinate technical staff members in all areas of polysomnography, performance testing, and actigraphy, and additional functions to include (but not limited to) PC-based initialization of devices with appropriate parameters and power sources; data acquisition; and data processing. * Design graphics for display of study designs, signals, processed data, etc. as necessary for manuscripts for publication in refereed journals, poster presentations, technical publications, instructional manuals, etc. Major Duties and Qualifications: The Researcher will manage/Coordinate Human Studies in Sleep Loss and Performance. Therefore, the Researcher: * Must have knowledge and skills in Psychology and Sleep Deprivation research. * Must have knowledge and ability to assist in Subject recruitment and physicals, including administration of standardized psychological evaluations. * Must have knowledge and skills necessary to train research assistants responsible for executing tasks required by the study, including but not limited to driving simulators, psychomotor vigilance tasks, ANAM, and MWT/MSLT. * Must have knowledge and ability to personally perform any tasks necessary for an experiment including those mentioned above, initializing and downloading actigraphs and other data, scoring polysomnographic variables for sleep, and other skills as needed for specific studies. The Researcher will perform statistical Analysis of Research Data * Must have knowledge and ability to collect, process, and prepare data for computer entry. * Must possess knowledge and ability to create computer database files for the purpose of analyses and archiving. * Must possess knowledge of, and skills/ability in, statistics and statistical packages for the purpose of data analyses and database management. The Researcher will prepare Abstracts and Presentations * Must have knowledge of psychology necessary to understand research objectives. * Must have ability to formulate and organize ideas in order to design coherent manuscripts. * Must possess knowledge of and skills in presentation techniques including design, construction, and actual presentation (i.e., public speaking) skills. The Researcher will collaborate With Others in the Creation of Papers for the Purpose of Publication * Must have knowledge and ability to incorporate computer generated displays into a written document. * Must have knowledge and understanding of relevant databases and accompanying analyses. QUALIFICATIONS *Advanced Degree (Masters, PhD or MD) desired, Bachelors or RN required *2-4 years knowledge and experience with Department of Defense (DoD) Grants and Agreements administration and management, preferred * 2-4 years Medical research project management experience strongly desired, preferably with Department of Defense * Experience with advanced medical technologies, preferred * Knowledge of military system, preferred. * Demonstrate competence in oral and written communication * Must be organized, attentive to detail, and posses a positive, friendly and professional demeanor * Ability to be flexible with changing priorities and available to interact with employees, clients and sponsors of all levels * Ability to exercise independent judgment in fast-paced, high-pressured environment with strict deadlines and to manage multiple projects * Ability to develop strong trusting relationships in order to gain support and achieve results * Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software

Field Data Collection Research Coordinator - Washington D.C., DC

Study Coordinator - Washington D.C. , DC

Study Coordinator (Non-Supervisory) - Washington D.C., DC

Researcher (Neurology) - Washington D.C., DC

DESCRIPTION Looking for an exciting new career? Join our team! The Geneva Foundation is a non-profit organization which promotes and supports military medicine. The Foundation has built relationships with highly skilled, exceptionally motivated, world-recognized researchers and medical professionals and hires top-quality staff. By joining The Geneva Foundation, you will have an exciting and stimulating career in which you will advance, "The Future of Military Medicine. Today." The Researcher (Neurology) main job is to provide services for the Department of Behavioral Biology, WRAIR, research program. The work will be performed primarily in the Washington D.C. metropolitan region, specifically at Walter Reed Army Institute of Research (WRAIR). The Researcher (Neurology) shall prepare and obtain approvals for human scientific protocols to investigate the relationships between sleep parameters and cognitive performance, alertness, personality, and militarily relevant disorders (e.g., PTSD, mTBI) - in accordance with department mission requirements and in support of the recently reorganized Physiological Health Program Area and the Psychological Health Program Area of the Military Operational Medicine Research Area Directorate (RAD III). The Researcher (Neurology) shall collect and analyze data and present preliminary findings at military, national, and international scientific conferences. Researcher (Neurology)shall also serve as authors or coauthors on manuscripts resulting from these data collection efforts. The Researcher (Neurology) shall assist other researchers in the Department of Behavioral Biology, WRAIR, involved in RAD III-related scientific investigations through discussion, site visits, and collaborative efforts and participate in department and research team meetings and conferences. DUTIES *Provide scientific expertise in psychophysiology, actigraphy, cognitive performance testing, personality testing, neurophysiology, statistical packages, functional brain imaging and advanced statistical techniques such as discontinuous growth modeling. *Will perform human research studies (field and laboratory) to include writing protocols, executing protocols, analyzing data, and writing manuscripts. *Travel as part of duties to locations inside and possibly outside of continental United States. Travel will be for purposes of developing collaborations, executing research, and participating in scientific meetings/symposia, etc.. *Will perform literature searches and literature reviews as part of protocol development and manuscript writing process. Must be comfortable with written English and capable of writing in scientific prose. Important in this job will be writing and submitting for publication scientific research. *Will perform standard and advanced statistics, using computer-based programs such as SAS, BMDP, etc. Must be familiar with standard Microsoft programs such as Excel, Word, Access, and PowerPoint. *Will work independently and with minimal supervision. Must also be able to function effectively as a member of an interdisciplinary team composed of researchers from a variety of backgrounds/institutions including WRAIR, MRMC, NIH, various universities, etc. *Will provide technical support in actigraph utilization for all research studies (field and laboratory) to include maintenance, testing, trouble-shooting, and repair of actigraphs. *Will train, lead, and/or coordinate technical staff members in all areas of polysomnography, performance testing, and actigraphy, and additional functions to include (but not limited to) PC-based initialization of devices with appropriate parameters and power sources; data acquisition; and data processing. *Will design graphics for display of study designs, signals, processed data, etc. as necessary for manuscripts for publication in refereed journals, poster presentations, technical publications, instructional manuals, etc. MajorDuties and Qualifications Will manage/coordinate Human Studies in Sleep Loss and Performance. Therefore, the Researcher will have the following: a. Knowledge and skills in Psychology and Sleep Deprivation research. b. Knowledge and ability to assist in Subject recruitment and physicals, including administration of standardized psychological evaluations. c. Knowledge and skills necessary to train research assistants responsible for executing tasks required by the study, including but not limited to driving simulators, psychomotor vigilance tasks, ANAM, and MWT/MSLT. d. Knowledge and ability to personally perform any tasks necessary for an experiment including those mentioned above, initializing and downloading actigraphs and other data, scoring polysomnographic variables for sleep, and other skills as needed for specific studies. Will conduct Statistical Analysis of Research Data, therefore the Researcher will have: a. Knowledge and ability to collect, process, and prepare data for computer entry. b. Knowledge and ability to create computer database files for the purpose of analyses and archiving. c. Knowledge of, and skills/ability in, statistics and statistical packages for the purpose of data analyses and database management. Will prepare Abstracts and Presentations, therefore the Researcher will have: a. Knowledge of psychology necessary to understand research objectives. b. Ability to formulate and organize ideas in order to design coherent manuscripts. c. Knowledge of and skills in presentation techniques including design, construction, and actual presentation (i.e., public speaking) skills. Will collaborate With Others in the Creation of Papers for the Purpose of Publication, therefore, the Researcher will have: a. Knowledge and ability to incorporate computer generated displays into a written document. b. Knowledge and understanding of relevant databases and accompanying analyses. &8195; QUALIFICATIONS *Advanced Degree (Masters, PhD or MD) in the areas of Neurology or related discipline desired, Bachelors or RN required * 2-4 years knowledge and experience with Department of Defense (DoD) Grants and Agreements administration and management, preferred * 2-4 years Medical research project management experience strongly desired, preferably with Department of Defense * Experience with advanced medical technologies, preferred * Knowledge of military system, preferred. * Demonstrate competence in oral and written communication * Must be organized, attentive to detail, and posses a positive, friendly and professional demeanor * Ability to be flexible with changing priorities and available to interact with employees, clients and sponsors of all levels * Ability to exercise independent judgment in fast-paced, high-pressured environment with strict deadlines and to manage multiple projects * Ability to develop strong trusting relationships in order to gain support and achieve results * Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software

Researcher (Statistical) - Washinton D.C., DC

DESCRIPTION Looking for an exciting new career? Join our team! The Geneva Foundation is a non-profit organization which promotes and supports military medicine. The Foundation has built relationships with highly skilled, exceptionally motivated, world-recognized researchers and medical professionals and hires top-quality staff. By joining The Geneva Foundation, you will have an exciting and stimulating career in which you will advance, "The Future of Military Medicine. Today." The Researcher (Statistical) main job is to provide services for the Department of Behavioral Biology, WRAIR, research program. The work will be performed primarily in the Washington D.C. metropolitan region, specifically at Walter Reed Army Institute of Research (WRAIR). DUTIES The Researcher (Statistical) shall prepare and obtain approvals for human scientific protocols to investigate the relationships between sleep parameters and cognitive performance, alertness, personality, and militarily relevant disorders (e.g., PTSD, mTBI) - in accordance with department mission requirements and in support of the recently reorganized Physiological Health Program Area and the Psychological Health Program Area of the Military Operational Medicine Research Area Directorate (RAD III). The Researcher (Statistical) shall collect and analyze data and present preliminary findings at military, national, and international scientific conferences. Researcher (Statistical) shall also serve as authors or coauthors on manuscripts resulting from these data collection efforts. The Researcher (Statistical) shall assist other researchers in the Department of Behavioral Biology, WRAIR, involved in RAD III-related scientific investigations through discussion, site visits, and collaborative efforts and participate in department and research team meetings and conferences. The Researcher (Statistical) shall be capable of performing the following tasks: 1. Provide advanced statistical techniques such as discontinuous growth modeling. Perform human research studies (field and laboratory) to include writing protocols, executing protocols, analyzing data, and writing manuscripts. 2. Travel as part of duties to locations inside and possibly outside of continental United States. Travel will be for purposes of developing collaborations, executing research, and participating in scientific meetings/symposia, etc.. 3. Perform literature searches and literature reviews as part of protocol development and manuscript writing process. Therefore must be comfortable with written English and capable of writing in scientific prose. Important in this job will be writing and submitting for publication scientific research. 4. Perform standard and advanced statistics, using computer-based programs such as SAS, BMDP, etc. 5. Must be able to work independently and with minimal supervision. Must also be able to function effectively as a member of an interdisciplinary team composed of researchers from a variety of backgrounds/institutions including WRAIR, MRMC, NIH, various universities, etc. 6. Provide technical support in actigraph utilization for all research studies (field and laboratory) to include maintenance, testing, trouble-shooting, and repair of actigraphs. 7. Must be able to train, lead, and/or coordinate technical staff members in all areas of polysomnography, performance testing, and actigraphy, and additional functions to include (but not limited to) PC-based initialization of devices with appropriate parameters and power sources; data acquisition; and data processing. 8. Design graphics for display of study designs, signals, processed data, etc. as necessary for manuscripts for publication in refereed journals, poster presentations, technical publications, instructional manuals, etc. Other major duties and qualifications include: *Assist in Managing/Coordinating Human Studies in Sleep Loss and Performance Will be adept at Psychology and Sleep Deprivation research. *Must have knowledge and ability to assist in Subject recruitment and physicals, including administration of standardized psychological evaluations. *Must possess knowledge and skills necessary to train research assistants responsible for executing tasks required by the study, including but not limited to driving simulators, psychomotor vigilance tasks, ANAM, and MWT/MSLT. *Must have knowledge and ability to personally perform any tasks necessary for an experiment including those mentioned above, initializing and downloading actigraphs and other data, scoring polysomnographic variables for sleep, and other skills as needed for specific studies. Will be required to do Statistical Analysis of Research Data, therefore the Researcher will: *Possess knowledge and ability to collect, process, and prepare data for computer entry. *Have knowledge and ability to create computer database files for the purpose of analyses and archiving. *Will have knowledge of, and skills/ability in, statistics and statistical packages for the purpose of data analyses and database management. Prepare Abstracts and Presentations *Must have knowledge of psychology necessary to understand research objectives. *Must have ability to formulate and organize ideas in order to design coherent manuscripts. Must have knowledge of and skills in presentation techniques including design, construction, and actual presentation (i.e., public speaking) skills. Collaborate With Others in the Creation of Papers for the Purpose of Publication *Must have knowledge and ability to incorporate computer generated displays into a written document. *Must have knowledge and understanding of relevant databases and accompanying analyses. QUALIFICATIONS Advanced Degree (Masters, PhD or MD) desired, Bachelors or RN required *Expert knowledge of SAS statistical software * 2-4 years knowledge and experience with Department of Defense (DoD) Grants and Agreements administration and management, preferred * 2-4 years Medical research project management experience strongly desired, preferably with Department of Defense * Experience with advanced medical technologies, preferred * Knowledge of military system, preferred. * Demonstrate competence in oral and written communication * Must be organized, attentive to detail, and posses a positive, friendly and professional demeanor * Ability to be flexible with changing priorities and available to interact with employees, clients and sponsors of all levels * Ability to exercise independent judgment in fast-paced, high-pressured environment with strict deadlines and to manage multiple projects * Ability to develop strong trusting relationships in order to gain support and achieve results * Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software

Research Statistician - Silver Spring, MD

Research Assistant I - Atlanta, GA

Human Resources Assistant - Tacoma, WA

Grants & Contracts Manager - Tacoma, WA

Pre Award Manager - Tacoma, WA

Social Work Care Manager - Ft. Stewart, GA, GA

Postdoctoral Fellow (T2) - Tacoma, WA

Research Coordinator - Landstuhl, Rhineland-Palatinate

Research Coordinator - Honolulu, HI

Research Nurse / Project Director - San Antonio, TX

DESCRIPTION This study is examining is examining the effectiveness of an oral care program, education and implementation of an evidence-based oral care clinical guideline to determine whether it results in increased knowledge and improved oral care practices and compliance. The Research Nurse / Project Director provides technical knowledge and expertise in nursing care to support the development of evidence-based programs. This position will assist with participant recruitment, participant screening, data collection, and compilation of study results. This individual must be comfortable speaking in front of large groups of people. Additionally, the Research Nurse / Project Director will assume patient care assignments for ICU Nurse Champions when teaching the Innovative Oral Care Education classes along with members of the project team. This position effort is a minimum of 20 hours per week. Hours will vary depending on the time of patient consent; candidate will need to be flexible with hours they're available. Research will take place at the United States Army Institute of Surgical Research and Brooke Army Medical Center. DUTIES Responsibilities: * Provide technical knowledge and expertise in nursing care * Perform preliminary research, information gathering and packaging * Promote safety and confidentiality of research participants at all times * Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practice (GCP) and infection control procedures, when applicable * Participate in the hiring, training and supervision of other research personnel as applicable * Maintain a collaborative research environment between the Principal Investigator (PI), other site personnel, research participants, The Geneva Foundation and the funding organization * Prepare for research study to include regulatory submission process * Execution and maintenance of research study * Manage study documentation * Oversee subject recruitment and enrollment, as needed * Conduct research subject visits as directed * Collect data and complete data entry process * Prepare interim and final progress reports * Document all correspondence and communication pertinent to the research * Procurement of supplies and equipment as authorized per research budget guidelines * Participate in the analysis of the data and the preparation of the manuscript * Maintain an updated literature library of journal articles related to the research topic * Maintain the security and confidentiality of all research records * Perform duties necessary to comply with and implement research study protocol * Maintain and update files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.) QUALIFICATIONS * Bachelors or R.N. required * 1-2 years medical research project management experience strongly desired, preferably with Department of Defense * 1-2 years non-profit, research, or healthcare experience desired * Knowledge of military system, preferred * Demonstrate competence in oral and written communication * Must be organized, attentive to detail, and posses a positive, friendly and professional demeanor * Ability to be flexible with changing priorities and available to interact with employees, clients and sponsors of all levels * Ability to exercise independent judgment in fast-paced, high-pressured environment with strict deadlines and to manage multiple projects * Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software * Ability to perform triage, patient assessment and nursing care functions * Data mining, administering medication, operating specialized medical equipment experience, strongly desired * Knowledge of preoperative assessment, intraoperative phase, and postoperative evaluation, desired * Knowledge of emergency measures, use and affects of intravenous fluids, normal and abnormal responses to anesthetics, and effects, side effects and complications by pharmaceuticals, preferred

Research Coordinator - Landstuhl, Rhineland-Palatinate

Research Assistant - San Diego, CA

DESCRIPTION The study is testing the safety and efficacy of virtual reality based treatments for Post Traumatic Stress Disorder (PTSD) in Service Members with PTSD from combat in Iraq and Afghanistan. The Research Assistant will assist with recruiting, performing independent assessments on subjects, collecting and organizing data, and performing administrative tasks in support of the overall project. The position is estimated at 20 hours per week. Human research subject training required upon employment. DUTIES Responsibilities: * Promote safety and confidentiality of research participants at all times * Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures * Manage study documentation to include accurate and timely filing * Comply with all the rules and regulations as applicable to assigned duty station * Assist in all phases of the research project * Recruit research participants, assist in enrollment and protocol procedures, monitor follow-up visits, oversee regulatory and administrative details, and provide data management assistance and project close-out support as applicable * Will be required to travel, using personnel vehicle, between NMCSD and Camp Pendleton on a frequent basis. Will be responsible for tracking mileage using a mileage log. Mileage will be reimbursed at the government approved rate. QUALIFICATIONS * Bachelors degree or equivalent work experience required * 1 year experience in research preferred * Non-profit, research, or healthcare experience desired * Demonstrate competence in oral and written communication * Must be organized, attentive to detail, and posses a positive, friendly and professional demeanor * Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner * Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software

Research Coordinator - San Diego, CA

DESCRIPTION The role of the Coordiantor is to work with the Principal Investigator to manage and coordinate the clinical research protocol at their Military Treatment Facility (MTF). The Coordinator will assist with subject enrollment, data collection, monitor follow-up visits, regulatory and administrative details, provide data management assistance and project close-out support. This position will begin as part-time at approximately 16-20 hours per week. The Research Coordinator will support multiple protocols in this position and as each protocol receives regulatory approvals, this position will transition to full-time (approximately 32 - 40 hours per week). DUTIES Research Study Responsibilities: * Promote safety and confidentiality of research subjects at all times * Proactively prepare for study initiations * Meet or exceed sponsor and Geneva enrollment, study execution, and monitoring expectations * Conduct a minimum average of 10 study visits per week - 40 visits per month * Support and assist team members in completing other trials * Demonstrate competency and accuracy in completing source documentation and CRFs * Report and document Adverse Events (AEs) and Serious Adverse Events (SAEs) per sponsor requirements * Maintain complete and accurate drug accountability at all times * Demonstrates proficiency in performing basic study related procedures (i.e., Vital Signs, ECG, phlebotomy) as required * Proficiently perform appropriate study specific procedures (i.e., PFTs, phlebotomy, glucometers, remote data entry, special lab processing) * Be cognizant of and adhere to FDA and OSHA regulations and GCP guidelines QUALIFICATIONS * RN or LPN preferred * CRC preferred * FDA regulated clinical research experience using GCP, ICG Guidelines required * Fully proficient in medical terminology and abbreviations * Knowledge of military system preferred * Ability to operate independently * Ability to organize and secure study files * Demonstrated competence in oral and written communication * Computer skills including knowledge of Microsoft Word, Excel, Access and e-mail

Research Coordinator - Washington D.C., DC

DESCRIPTION The Research Coordinator oversees and administers research study and associated activities. Assists in project planning, and ensures that pre-established work scope, study protocol and regulatory requirements are followed. May recruit and coordinate research subjects, as appropriate, and serves as principle administration liaison for the project. Oversees and coordinates the provision of administrative and staff services to investigators; develops and maintains record keeping systems and procedures. This study will examine the prevalence of hypopituitarism following combat-related traumatic brain injury (TBI). The ideal candidate will have the following: - current nursing license - experience with IV Therapy (and hold current, applicable certifications) - experience with timed serial blood draws DUTIES Responsibilities for the Research Coordinator includes, but not limited to: - Promote safety and confidentiality of research participants at all times - Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures - Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures - Plan, implement and maintain data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data - Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope - Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives - Organize and facilitate meetings, conferences, and other events associated with research activities; may perform and/or coordinate outreach activities, as appropriate to research objectives - Document all correspondence and communication pertinent to the research - Interact and communicate effectively with Principal Investigator, other site personnel, research participants, The Geneva Foundation, and the funding organization - Comply with all the rules and regulations as applicable to assigned duty station QUALIFICATIONS - Bachelors degree or equivalent work experience required - RN or LVN license required - Experience with IV Therapy and have current, applicable certification required - Experience with metabolic testing preferred - Experience with timed serial blood draws required - 2-4 years experience in clinical research preferred - 2-4 years non-profit, research, or healthcare experience desired - Demonstrate competence in oral and written communication - Must be organized, attentive to detail, and posses a positive, friendly and professional demeanor - Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner - Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software - Knowledge of CFR, GCP and ICH guidelines

Quality Assurance Specialist - Frederick, MD

DESCRIPTION This position is for an upcoming opportunity. This position is responsible for reviewing procedures, compliance survey development, surveying laboratory personnel, and writing Standard Operating Procedures (SOPs) under a firm delivery schedule. The ideal candidate will be Bachelor's prepared. Specific tasks: - Obtain current procedures utilized by the laboratory facility from appropriate POC - Review facility's existing procedures to determine whether compliance updates are needed - Identify any inaccurate or noncompliant components and ensure changes are made and incorporated into corresponding SOPs - Develop a compliance survey and distribute to appropriate laboratory personnel - Draft SOPs utilizing appropriate laboratory format - Work with the QA team to ensure deliverables are submitted in a timely manner incorporating all customer and team comments. DUTIES Responsibilities: - Promote quality achievement and performance improvement throughout the organization - Ensure QA compliance objectives and targets are achieved - Maintaining awareness of the business context and budgetary control issues - Ensure compliance with national and international standards and legislation - Consider the application of environmental and health and safety standard - Agree standards are clearly defined quality methods for staff to apply - Define quality procedures in conjunction with operating staff QUALIFICATIONS - Bachelors' degree or equivalent work experience required - Must be a U.S. Citizen due to site restrictions - 4 years' experience in quality assurance required - 2-4 years non-profit, research, or healthcare experience desired - Demonstrate competence in oral and written communication - Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor - Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner - Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software

Quality Assurance Scientist - Frederick, MD

DESCRIPTION This position is for an upcoming opportunity. This position is responsible for reviewing procedures, compliance survey development, surveying laboratory personnel, and writing Standard Operating Procedures (SOPs) under a firm delivery schedule. The ideal candidate will be doctoral-prepared. This position will supervise the performance of the following tasks: - Obtain current procedures utilized by the laboratory facility from appropriate POC - Review facility's existing procedures to determine whether compliance updates are needed - Identify any inaccurate or noncompliant components and ensure changes are made and incorporated into corresponding SOPs - Develop a compliance survey and distribute to appropriate laboratory personnel - Draft SOPs utilizing appropriate laboratory format DUTIES Responsibilities: - Promote quality achievement and performance improvement throughout the organization - Ensure QA compliance objectives and targets are achieved - Maintaining awareness of the business context and budgetary control issues - Ensure compliance with national and international standards and legislation - Consider the application of environmental and health and safety standard - Agree standards are clearly defined quality methods for staff to apply - Define quality procedures in conjunction with operating staff QUALIFICATIONS - PhD or MD prepared or equivalent work experience required - Must be a U.S. Citizen due to site restrictions - 4 years' experience in quality assurance experience preferred - 2-4 years non-profit, research, or healthcare experience desired - Demonstrate competence in oral and written communication - Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor - Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner - Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software

Identified Candidate - Tacoma, WA

DESCRIPTION If you have been asked to apply for a specific position, please fill out this application.