Clinical Trial Liaison

JobsCloseBy Editorial Insights

PSI CRO is seeking a Clinical Trial Liaison in Zug to act as the on-site face of PSI, helping sites identify and recruit patients through protocol focused support. The role is about serving as a specialized liaison to optimize patient enrolment, coordinating site recruitment plans aligned with study metrics, and sharing recruitment expertise with site staff and monitors. Qualifications include RN, Pharmacist, or Physician with at least 5 years of clinical practice and experience in Oncology, Gastroenterology, or Neurology; English proficiency with German or French a plus; strong MS Office skills; and excellent interpersonal and presentation abilities. Tips for applicants: tailor your CV to highlight proven recruitment successes, quantify outcomes, show cross-functional collaboration and protocol review experience, and confirm willingness to work onsite in Zug and contribute to BD proposals.

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 (proficiency in German and/or French language 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.