Freelance Senior Clinical Research Associate
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Freelance Senior Clinical Research Associate
- Full-time
PSI is a leading Contract Research Organisation with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
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 beon 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
- Supervisingstudy 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
- BSc or MSc in Life Sciences (or similar),or an equivalent combination of education, training & experience
- Independent on-site monitoring experience in Belgium, ideally onmultiple projects at a time
- Demonstrable experience in all types of monitoring visits in Phase II and/or III
- Experience supporting Oncology/ Hematologyand Infectious disease studies
- Fluencyin 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
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