Bordet - Project Manager Clinical Trials Center
Il y a 6 mois
**Fonction**:
The primary role of the Project Manager is to administer, maintain and co-ordinate various logístical aspects of clinical trials in accordance with standards procedures and guidelines. The PM acts as a pivotal point of contact for the study team.
**Tasks and Responsibilities**:
- Organise study set-up activities;
- Ensure that milestones, deliverables, quality and timelines are met within budget and in accordance with regulatory and contractual requirement;
- Write or contribute to preparation of study protocol, informed consent forms and any other clinical research related documents;
- Coordinate investigational medicinal product (IMP) supplies
- Assist with Ethics Committees and/or Competent Authorities submissions and filing necessary supportive documentation
- Ensure studies are carried out according to the study protocol, SOPs, and ICH GCP regulations and study specific manuals and procedures
- Report risks/issues that can affect the study and work to the study team to implement corrective actions
- Ensure appropriate filing of study documents in the trial master file
**Profil**:
- Holds a master degree in the scientific, biomedical or paramedical field
- Experience of working on clinical trials with knowledge of GCP
- Excellent command of written & spoken English, as well as French or Dutch.
- Ability to make decisions
- Team player, strong diplomatic skills
- Willing to bring his/her contribution in a demanding academic environment
**Offre**:
- A full time undertermined contract
- An attractive salary with extra-legal advantages
- Proximity with a metro station, free parking.
**Interested?
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