Freelance Senior Clinical Research Associate
PSI CRO
•Onsite
About The Position
As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring 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. This is a freelance (contractor) position in Belgium.
Requirements
- BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
- Independent on-site monitoring experience in Belgium, 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
- Full and clean driver's license, and the ability to travel
- Intermediate to Advanced knowledge of MS Office
Responsibilities
- Conducting and reporting all types of onsite monitoring visits
- Performing CRF reviews, source document verification and query resolution
- Be responsible for site communication and management
- Supervising study activities, timelines, and schedules for each site
- Acting as a point of contact for in-house support services and vendors
- Supporting quality control, such as compliance monitoring and reports review
Benefits
- Invests in their professional development and success
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What This Job Offers
Career Level
Senior
Education Level
Associate degree
