Freelance Senior Clinical Research Associate

PSI CRO·Brussels, Brussels, Belgium

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About the role

Freelance Senior Clinical Research Associate contractor role in Belgium. The position involves on-site monitoring, CRF review, source document verification, query resolution, site management, study oversight and quality control across Phase II/III studies. Candidates need relevant life-sciences education or an equivalent route, Belgian on-site monitoring experience, oncology/hematology and infectious-disease study experience, Dutch and English fluency, professional French, a clean driving licence and travel availability.

Key requirements

• BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
• Required skills: Independent on-site monitoring experience in Belgium, Experience in all types of monitoring visits in Phase II and/or III studies, Experience supporting Oncology/Hematology and Infectious disease studies, Site communication and management, CRF review, Source document verification, Query resolution, Study activity, timeline and schedule supervision, Quality control and compliance monitoring, Intermediate to Advanced knowledge of MS Office, Ability to travel
• Required languages: Dutch, English, French
• Professional registration/licence (Belgium)

Opportunity details

• Workplace: Hybrid
• Employment: Contract
• Posted: Sep 15, 2026
• Original advert language: English

Full vacancy

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Employer’s role description

Job title: Freelance Senior Clinical Research Associate

Location: Brussels, Brussels, Belgium

Employment type: Full-time

Company Description

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.

Job Description

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 driver's 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 we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.