Are you an experienced freelance Clinical Project Manager with very good knowledge of Dutch, French, and English?
Do you have strong operational skills and availability for a 1-year contract?
Can you commit to a full-time or 80% hybrid role (2 days/week on-site in the Brussels area)?
If so, don't hesitate - apply now!
Job Description
As a Freelance Clinical Project Manager, you will be responsible to ensure successful execution of clinical studies in Belgium.
Responsibilities
- To focus on the daily operational tasks and successful FU of clinical studies in Belgium
- To provide leadership and guidance to the local study team (CRAs): to meet timelines, patient recruitment and monitoring Operational tasks: to oversee all aspects of the clinical studies, to keep systems up to date (Veeva), budgets and payments (this does not entail IRB/IEC Submissions and also not contract negotiations)
- Quality: to ensure an effective and efficient execution in accordance to ICH-GCP, SOPs and local regulations, inclusive eTMF review
- Stakeholder management: relations with investigators, sites and representations of the global study team in Belgium
Requirements
- University degree or equivalent; preferably in a medical/science-related field
- At least 10 years clinical experience
- Communication: excellent written and verbal communication skills in Dutch, in French and in English
- Open mindset to work on different tasks to be able to meet study timelines
- Eagerness to learn
- Organizing: demonstrated ability to prioritize and manage multiple tasks, self-motivated and achievement driven
- Problem-solving skills
- Good knowledge of ICH GCP, SOPs/Guidelines and quality standards related to study management
Contract information
- 1 year contract
- Full-time, 90% or 80%
- Hybrid model : 2 days/week on-site at client's location (Brussels area)
- Start-date : ASAP (January 5th the latest)
