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CLINICAL TRIAL ASSOCIATE (CLINICAL OPERATIONS EUROPE)
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| Titre |
CLINICAL TRIAL ASSOCIATE (CLINICAL OPERATIONS EUROPE) |
| Description |
Key Responsibilities: - Review clinical study documents for accuracy and completeness. - Participate in Study Team meetings and write minutes. - Enter study information into Clinical Trial Management System. - Review/Submit for archiving (TMF) all study documents on an ongoing basis. - Ensure TMF is up-to-date for assigned projects. - Assist in monitoring of timelines and resources (e.g. identification of budget deviations). - Liaise with CRAs and site coordinators to resolve queries. - Assist in the development of monitoring tools. - Monitor and direct supply/re-supply study drug shipments to investigational sites as appropriate. - Interface with vendors on ordering of non-drug trial supplies (e.g. CRFs). - Assist Clinical Operations Manager as needed in support of assigned projects. Your Profile: - BS degree in health science or scientific discipline. - At least 3 years experience as a Clinical Trials Associate or similar experience. - Knowledge of medical terminology. - Valid Swiss working permission or EU Citizenship required. - Knowledge of regulatory environment (FDA, ICH, GCP). - Excellent written and oral communication skills. - Knowledge of medical terminology. MICHAEL PAGE CONTACT : Your application will be sent to Terence O'Hare (Zurich Office), pease quote the job reference KTOH19654 Our client is a top biopharmaceutical company focussed on improving healthcare through innovative and effective drug development. They are currently looking for a Clinical Trial Associate (Clinical Operations Europe). |
| Pays |
France |
| Date de publication |
19 juin 2007 |
| Société ou Annonceur |
Michael Page |
| secteur activité |
Biotechnologies |
| Qualification |
International |
| Type de contrat |
CDI |
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