Freelance Senior Clinical Research Associate

PSI CRO · Brussels, Brussels, Belgium · posted Sep 15, 2026

Open to candidates in Belgium

Full-timesenior

What this role actually asks for

Extracted by RemoteHunt

Must have

  • Independent on-site monitoring experience in Belgium
  • Experience in all types of monitoring visits (Phase II/III)
  • Fluency in Dutch and English
  • Professional proficiency in French
  • Full and clean driver's license
  • Ability to travel

Nice to have

  • Experience on multiple projects
  • Experience supporting Oncology/Hematology/Infectious disease studies

Tools and technologies

MS Office

Languages required

nlenfr

Worth checking before you apply

  • freelance

The full posting

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.

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