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 on-site, you will be a key contributor to the success of clinical trials and a trusted resource for site teams.
Responsibilities
* 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.
Requirements
* 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.
Benefits
* Indefinitie duration contract
* Hybrid policy: 2 days in the office in Leuven, 3 days homeworking