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, Dutch and French
* 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.