Clinical Project Manager (VAC/164)
Email this Job offerRegion: Regional
Sector: Pharmaceutical Industry
Type of contract: Permanent - Full Time
Category: Clinical trials
For leading pharmaceutical, biotechnology or medical devices company's.
Description
The Clinical Project Manager (CPM) ensures that clinical trials are effectively executed at a country/sub-regional level, from pre-study through close-out activities.
Responsibilities:
• Manage pre-selection and trial initiation activities;
• Ensure trials are completed within budget, timeline, and enrolment commitments, and that the SOPs are followed;
• Co-monitor sites to track progress;
• Supervise on the proper maintenance of regulatory documentation;
• Tracking drug and clinical trial supplies;
• Ensure contracts are in place;
• Perform trial close-out activities.
Profile
• Medical, paramedical or scientific study background;
• Very good knowledge and respect of GCP/SOPs;
• Good interpersonal communication skills in English, Dutch and French;
• Autonomous and Accurate self-starter with good organization skills;
• Proactive, shows initiative and positive team spirit;
• Computer literate.
Experience
Up to 5 years of experience in clinical monitoring, a first project management experience is an asset.
Languages
English: Very GoodDutch: Good
French: Good
German: Not applicable
