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Flemish BrabantHybrid36 hours/week<3months
You will be welcomed into a globally operating organization where team spirit is key.
What you do
- You will work on the frontline of communication with project stakeholders.
- You will ensure timelines, targets, and standards of clinical research projects in a variety of therapeutic indications.
- You will build and maintain relationships with clinical sites and investigators.
- Your focus will be on subjects' rights, safety, and well-being, and quality of data compliance.
- You will conduct and report all types of onsite monitoring visits.
- You will perform CRF reviews, source document verification, and query resolution.
- You will be responsible for site communication and management.
- You will supervise study activities, timelines, and schedules for each site.
- You will act as a point of contact for in-house support services and vendors.
- You will support quality control, such as compliance monitoring and reports review.
What they ask
- A BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience.
- Independent on-site monitoring experience, ideally on multiple projects at a time.
- Demonstrable experience in all types of monitoring visits in Phase II and/or III.
- Experience supporting Oncology/Hematology and Infectious disease studies.
- Fluency in Dutch and English, with professional proficiency in French.
- A full and clean driver's license, and the ability to travel.
- Intermediate to Advanced knowledge of MS Office.
How to apply
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