Clinical Trial Liaison
2/6/2026
The Clinical Trial Liaison supports clinical sites by providing protocol-focused assistance to enhance patient identification and recruitment efficiency. This role involves guiding sites on enrolment techniques, coordinating recruitment and retention plans, and serving as the on-site representative for PSI.
Working Hours
40 hours/week
Company Size
1,001-5,000 employees
Language
English
Visa Sponsorship
No
Company Description
PSI is a leading Contract Research Organization with over 30 years on the market, 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 Clinical Trial Liaison, you will help clinical sites identify and recruit patients more efficiently by providing protocol‑focused support. Acting as the face of PSI on-site, you will be a key contributor to the success of our clinical trials and a trusted resource for site teams.
You will:
- Serve as a specialized liaison to support sites with a protocol‑tailored strategy that enhances patient identification and recruitment efficiency.
- Guide clinical sites in developing and implementing effective patient enrolment techniques.
- Coordinate site‑specific recruitment and retention plans, ensuring alignment with study metrics.
- Provide expertise and insights to site staff involved in patient recruitment activities.
- Monitor, track, and report patient enrolment progress throughout the study lifecycle.
- Review and analyze study protocols to identify opportunities to optimize the patient pathway.
- Support project teams by ensuring accurate documentation of study‑specific assessments related to patient enrolment.
- Advise and collaborate with site monitors on patient recruitment strategies.
- Supply patient‑enrolment insights to Business Development for proposals.
Qualifications
- Registered Nurse (RN), Pharmacist, or Physician
- Experience working in at least one of the therapeutic areas: Oncology, Gastroenterology, Neurology
- At least 5 years of relevant clinical practice experience, including patient‑enrolment strategies for clinical trials
- Full working proficiency in English and Dutch (proficiency in French is advantageous)
- Proficiency with MS Office
- Excellent interpersonal skills and the ability to build strong relationships with diverse stakeholders
- Self‑driven, with the ability to work both independently and collaboratively
- Strong communication and presentation abilities
Additional Information
If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.
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