Clinical Research Associate |
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| Compania: PAREXEL International |
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| Expirat la: 26.09.2006 |
| Actualizat la: 24.09.2006 |
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| Compania: |
PAREXEL International |
| Departament: |
Cercetare, Research, Studii Cantitative si Calitative, Chimie, Biochimie, Farmacie, Healthcare, MedicinaUmana, Veterinara, Stomatologie |
| Orasul: |
Bucuresti
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| Tip Job: |
Full time |
| Posturi disponibile: |
1 |
| Status: |
Inactiv |
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| Nivel cariera: |
Mid-Level/Peste 3 Ani Exp,Manager/Executive Position |
| Limbi Straine: |
engleza, |
| Oferta: |
nespecificat |
| Permis conducere: |
nespecificat |
| Data introducerii: |
26.08.2006 |
| Data limita: |
26.09.2006 |
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| CANDIDATUL IDEAL:
Qualifications:
• Education: Educated to degree level (biological science, pharmacy or other health related discipline preferred) or equivalent nursing qualification/experience.
• Minimum Work Requirements: Minimum of 2 years (EU) monitoring experience in clinical research.
• Skills:
o Client focused approach to work;
o Excellent interpersonal, verbal, and written communication skills, (including experience in making presentations);
o Flexibility towards work assignments, new learning and travel (overnight, weekend and occasional international travel may be required);
o Ability to manage multiple and varied tasks and prioritize workload with attention to detail;
o Willingness to work with multiple supervisors/colleagues in a matrix environment, and to value the importance of team work;
o IT literate ' Experience with Microsoft based applications and general knowledge of PC functions;
o Team player with outstanding interpersonal, negotiation skills and organisational skills;
o Able to take initiative and work independently; sense of urgency in completing assigned tasks;
o Holds a driving license;
o Competent in written and oral English.
| RESPONSABILITATI / BENEFICII:
We are looking for in several European locations
CLINICAL RESEARCH ASSOCIATES
The responsibility of a Clinical Research Associate is to perform the clinical monitoring aspect of designated projects in accordance with PAREXELs SOPs. As Regional CRA or Primary CRA (on smaller studies) responsibilities will also include managing clinical monitoring activities in addition to the ownership of investigator sites, including investigator/site selection, collating regulatory documentation, initiation and monitoring (source data verification, drug accountability and data collection) in accordance with ICH GCP guidelines.
If you are interested in working in a fast paced and rapidly changing environment, please send your CVs in English, a covering note describing what you have to offer PAREXEL and details of your salary expectation to: HR-Europe@parexel.com. | DESCRIEREA COMPANIEI:
For two decades, PAREXEL International has played a key role in the pharmaceutical, biotechnology and medical device industries by partnering with clients to accelerate time to market, control development costs, reduce risk and maximize return on investment. As one of the largest pharmaceutical services companies in the world, PAREXEL delivers a full range of services and solutions through its offices in 36 countries. |
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