Svoj CV dostaviti na email.

Za potrebe sektora za istra??ivanje tr??i??ta ??? Ninamedia Research ??? ogla??ava
konkurs za slede??u poziciju:

Anketar na terenu
Srbija

Zadu??enja: Odgovorno i na vreme obavljanje svih poverenih zadataka
Obavezno prisustvo instrukta??i
Saradnja sa terenskim instruktorom ??? kontrolorom
Anketiranje doma??instava na unapred odre??enom terenu i u jasno definisanim
rokovima
Stru??na znanja i iskustva:
Minimum SSS ;
Po??eljno je da kandidat ima iskustva u radu kao anketar ali nije neophodno
Po??eljno je znanje ma??askog, slova??kog ili rumunskog jezika na nivou verbalne
komunikacije kao i gestovnog govora Odgovornost, pouzdanost, spremnost na terenski rad

Na??eg budu??eg saradnika o??ekuju dobri uslovi za rad i adekvatna zarada.

Samo kandidati koji u??u u na?? u??i izbor bi??e kontaktirani.

Bi??ete pla??eni da obavite kupovinu i zatim nam date svoje mi??ljenje, te nam tako pomognete podi??i kvalitetu usluge.

International Service Check, me??unarodna kompanija za ispitivanje kvalitete usluge, tra??i kriti??na i odgovorna lica bez obzira na dob, za analizu usluge na razli??itim prodajnim lokacijama ??? pre svega u Kragujevcu, Jagodini, Kraljevu, Novom Pazaru, Para??inu, ??abcu, Apatinu, Vr??cu i Kikindi.

Prijave na:
http://www.internationalservicecheck.com/

Travelmed Group
Accommodation and Travel Network
Tel.: 018/200-760
Fax: 018/576-555
E-mail: hr@travelmed.gr
Regional Office: Radoja Domanovica 2, 18000, Nis, Serbia

Description:

Quality Assurance Specialist
Quality Assurance Specialists are needed for a national research project with an outstanding CRO nation wide.

Responsibilities include:

Managing and planning regulatory affairs compliance for industry sponsors and/or sites in networks. This position will work closely with the regulatory affairs management, department director and/or primary investigators to ensure compliance, preparing for auditing activities while meeting strict deadlines.

Background:

BSc is the minimum education level accepted for this position.
Previous experience in research required; oncology experience preferred.
Good Understanding of ICH GCP is necessary, GLP and GMP are an asset.

Ideal Candidate:

BSc is the minimum education level accepted for this position.

CV on English with photo and phone number send to serbia_new_job_team@yahoo.com
For future details candidates will appropriate technical support agent.

Description:
Data Manager
Clinical Data Managers are responsible for processing data associated with a clinical trail. We are currently looking for Data Managers across UK for a large project. Each DM will be responsible for 4-6 sites. Electronic Data Capture is necessary.
This position is conducted off site. You will be working from home, with some travel for conference purposes. This position offers very flexible hours.

Candidates should possess:
BSc in IT related Field, additional life science background is an asset.
Electronic Data Capture Experience is necessary
Knowledge of Good Clinical Practices
Good Written and Oral Communications Skills

Ideal Candidate:
BSc in IT related Field, additional life science background is an asset.
CV on English with photo and phone number send to serbia_new_job_team@yahoo.com
For future details candidates will appropriate technical support agent.

Description:
The Clinical Research Associate II performs routine site visits to ensure that the rights and well being of human subjects are protected; the reported trial data are accurate, complete, and verifiable from source documents; and that the conduct of the trial is in accordance with the currently approved protocol/amendment(s), SOPs, GCP/ICH Guidelines and other applicable regulatory requirements. In doing this, the Clinical Research Associate II represents the company and the sponsor to site personnel and colleagues with professionalism and integrity.

Ideal Candidate:
Qualifications – Bachelor‘s level degree in life sciences, pharmacy, nursing or RN preferred – Two to five years clinical monitoring experience – Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements – Ability to work independently in a fast-paced environment – Strong communication, interpersonal, and organizational skills – Must demonstrate good computer skills – Position requires approximately 60% travel (may be up to 80% during peak times) – Attention to detail Identifies and resolves discrepancies related to source documents and case report forms, and discrepancies within case report forms with the investigator and site staff. Notes and resolves errors in written documentation. – Communication, verbal Conveys thoughts in a clear, concise, and accurate manner. Uses correct grammar. Listens carefully and asks questions when necessary to ensure understanding. – Communication, written Conveys findings in a clear, concise, and accurate manner. Monitoring reports and follow-up letters require few clarifications or editions by project team. – Computer literacy Uses computer hardware and software as productivity tools in performing work-related tasks. Enters information into company-required tracking programs with minimal outside assistance. – Customer service Provides customers (clients and site personnel) with complete and accurate information. Quickly identifies needs and follows through on commitments made. Maintains a high energy level when interacting with customers. Demonstrates professionalism and presents a positive image of the company. – Development of self and others Identifies personal career development goals and opportunities related to current job with assistance of regional manager. – Seeks additional training and assistance with additional responsibilities and feedback on performance. – Planning & organizing Plans work effectively to meet goals and ensure timely completion of assignments. Manages time effectively. Has a routine or system for completing work. Consistently meets timelines. Proactively notifies manager of any difficulties with balancing workload. – Problem solving & decision making Demonstrates ability to make sound decisions. Focuses on resolving problems and makes decisions in a timely manner. Promptly notifies project team of the problem and any decisions made. – Relationship building Maintains positive relationships with site personnel and colleagues. Demonstrates honesty and integrity in dealing with others. – Resolves conflicts with others promptly and effectively. Accepts constructive feedback. – Technical knowledge Displays full knowledge of protocol, regulatory requirements, and company SOPs. Identifies, documents, and discusses protocol violations, regulatory non-compliance, and issues involving subject safety. Distinguishes between good practice and regulatory requirements. Applies knowledge into practice on-site. – Therapeutic knowledge Portrays good knowledge of the disease under study. Discusses the disease with site personnel and colleagues. Comprehends medical information received. If new therapeutic indication, learns the vital aspects of the disease without major difficulty. – Work habits Demonstrates commitment, dedication, cooperation, positive behavior, adaptability and flexibility with changes in responsibilities and duties. – Meets timelines and follows up without being prompted. Plans travel time well and makes effective use of time.
CV on English with photo and phone number send to serbia_new_job_team@yahoo.com
For future details candidates will appropriate technical support agent.

Description:
An excellent opportunity to join an international CRO as a Senior Clinical Research Associate in Serbia on a permanent basis.
Excellent opportunity to act as part project manager co-ordinating international studies.
Excellent opportunity, benefits and salary.

Ideal Candidate:
The ideal candidate will have a minimum of 2 years experience in Clinical Research with a background in medicine.
Excellent English
Excellent computer skills
Driving licence
CV on English with photo and phone number send to serbia_new_job_team@yahoo.com
For future details candidates will appropriate technical support agent.

Description:
For research and monitoring in newly planned clinical trials.

Ideal Candidate:
Registered nurses; knowledge of GCP and ICH.
CV on English with photo and phone number send to serbia_new_job_team@yahoo.com
For future details candidates will appropriate technical support agent.

Description:
Project planning, coordination of activities and organizational entities to keep projects on track; evaluation of patient numbers, data quality, GCP standards in Study Centers.

Ideal Candidate:
Post-secondary education in marketing or commerce. A Masters in Business Administration (MBA) is beneficial, as is a degree in a life sciences area.
CV on English with photo and phone number send to serbia_new_job_team@yahoo.com
For future details candidates will appropriate technical support agent.

Description:
Project Manager
We are currently looking for 3 project managers in the UK. The responsibilities of this position will include overseeing the progress of the trial activates.
Monitoring Clinical Research Associates, Data Managers and Quality Assurance Staff. Project Managers will also be responsible for application to Regulatory Authorities.
Candidates should possess:
MBA and/or several years experience in Clinical Research
Understanding of Good Clinical Practices
Very Good Communication Skills
The Ability to travel up to 75% of the time

Ideal Candidate:
MBA and/or several years experience in Clinical Research
CV on English with photo and phone number send to serbia_new_job_team@yahoo.com
For future details candidates will appropriate technical support agent.

Description:
Clinical Research Associate
A Clinical Research Associate is responsible for monitoring clinical sites as a part of a larger clinical trial. CRA‘s will initiate new sites, train clinic staff in the procedures of the project and liaise with clinical staff through the project. They will collect data from sites, and process accordingly. CRA‘s will be responsible to monitor Good Clinical Practice Compliance and report adverse events.
This position will require the CRA to visit the site for 1 initiation visit, up to 12 monitoring visits and 1 close out visit. Data processing, teleconferences, and other activities will be done off site
This position has very flexible hours, work from home opportunities, and opportunities for travel.

Candidates should have:
BSc in a life sciences field or be a registered nurse
Knowledge of Good Clinical Practices
Good Computer skills
Experience with Electronic Data Capture
Excellent Written and Oral Communication Skills

Ideal Candidate:
BSc in a life sciences field or be a registered nurse
Knowledge of Good Clinical Practices
CV on English with photo and phone number send to serbia_new_job_team@yahoo.com
For future details candidates will appropriate technical support agent.

Description:
An excellent opportunity to join an international CRO as a home-based Clinical Research Associate in Slovenia on a permanent basis.
Excellent opportunity, benefits and salary.

Ideal Candidate:
The ideal candidate should have a minimum of 2 years experience in Clinical Research with a background in medicine.
Excellent English
Excellent computer skills
Drving licence
CV on English with photo and phone number send to serbia_new_job_team@yahoo.com
For future details candidates will appropriate technical support agent.

Description:
Coordinates all aspects of the clinical monitoring process, research; also ideal
for students part-time.

Ideal Candidate:
Graduates in Life Sciences/Students.
CV on English with photo and phone number send to serbia_new_job_team@yahoo.com
For future details candidates will appropriate technical support agent.

Description:
QA procedures, manufacturing, packaging and Formulation Development in-process testing checks, sampling and others. Implementation of good laboratory (GLP), good clinical practices (GCP) and/or good manufacturing practices (GMP).

Ideal Candidate:
University degree, preferably in Quality Assurance, Engineering, Chemistry,
Biochemistry; Computer Sciences,
Pharmaceutical, biology, biomedical science; Business Administration,
University degree, preferably in Quality Assurance, Engineering, Chemistry,
microbiology; medicine; molecular biology; pharmacology.
CV on English with photo and phone number send to serbia_new_job_team@yahoo.com
For future details candidates will appropriate technical support agent.

Description:
Data collection from clinical trials (pharmaceuticals, biologics, or devices) on behalf of a sponsor. Maintaining the accuracy, integrity and security of complex, large computerized records system; applying knowledge of regulations, policies, protocols and/or procedures to control and maintain accurate records.

Ideal Candidate:
Database specialist degree, a Bachelor‘s degree in computer science or other information technology (IT) field;
Previous data entry experience and intermediate level skills using a range of software applications (such as Oracle, Oracle Clinical, SAS, SQL, Powerpoint, MS Excel, MS Word, Data and MS Access) is required.
CV on English with photo and phone number send to serbia_new_job_team@yahoo.com
For future details candidates will appropriate technical support agent.

FEDERAL OBEZBE??ENJE d.o.o ??A??AK – NI??

PRIVATE POLICING

www.federal.co.yu

Mail: denis.s@sezampro.yu

Mob. 064/884-3018 (Ni??)

Informacije na telefon: 064/142-85-32 – Ivan