Freelance Senior Clinical Research Associate

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.

Your main responsibilities will include:

• 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

Qualifications :

• 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 drivers license and the ability to travel
• Intermediate to Advanced knowledge of MS Office

Additional Information :

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success. Our recruitment process is easy and straightforward and well be there with you every step of the way. We will guide and support you with information making your experience as smooth as possible.

Remote Work :

Yes

Employment Type :

Full-time