Les offres d'emploi : Professions sociales - Santé ...

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...