Clinical Project Leader (VAC/167)
Email this Job offerRegion: International
Sector: Medical Devices
Type of contract: Permanent - Full Time
Category: Clinical trials
For a leading medical devices company.
Description
The CPL will develop, coordinate and implement research and administrative strategies essential to the successful management of clinical investigations.
Responsibilities may include:
• Investigator recruitment and vendor selection and management;
• Develop project-related materials and procedures in accordance with all applicable regulations and SOPs;
• Establish and manager project timelines, financial requirements and operating budget;
• Recommend (refinement of) guidelines in the collection of clinical data and administration of clinical investigations;
• Ensure that tracking databases and filing of study related documentation remain updated;
• Coordinate the development, review, submission and publication(s) of clinical study report(s);
• Establish and maintain effective working relationships with investigational sites;
• Coordinate and facilitate study communication plans;
• Conduct limited monitoring in order to keep in touch with any issues in the field.
Profile
• Strong communication skills (towards team, investigators, vendors…) in English, French and Dutch;
• Good working knowledge of GCP and applicable regulatory requirements;
• Energetic, well-organized team-player;
• Stress resistant with leadership capabilities;
• Strong sense of ethics & commitment;
• Willing to travel up to 20%.
Education
Medical, paramedical or scientific study background.
Experience
Experience in Clinical Research in the pharmaceutical and/or medical device industry, years of experience subject to type of degree (2 to 7 years).
Languages
English: Very GoodDutch: Good
French: Good
