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Full-time
bachelor degree
Posted 1d ago
~40 hrs/week
Responsibilities
The Trial Committee Manager oversees the end-to-end management of clinical trial committees, ensuring activities are executed efficiently and in compliance with quality standards. They serve as the central point of coordination for sponsors, committee members, and cross-functional teams throughout the clinical trial lifecycle.
Requirements
Candidates must hold a bachelor's degree in a relevant field and possess at least 3 years of experience in clinical research, preferably within a CRO environment. Strong project management, stakeholder coordination, and communication skills are essential for this role.
Full job description
Company Description
PSI is a global Contract Research Organization (CRO) with over 30 years of experience supporting clinical research around the world. We combine the stability of an established organization with the agility and innovation needed to advance modern clinical trials. Guided by a commitment to quality and on-time delivery, we partner with clients across a broad range of therapeutic areas while providing our employees with an environment where they can grow, contribute, and make a meaningful impact on global healthcare.
Job Description
The Trial Committee Manager oversees the end-to-end management of clinical trial committees (IDMC, Safety Review Committee, Adjudication Committee etc.) that provide unbiased oversight and expert guidance throughout the lifecycle of clinical trials. In this role, you will serve as the central point of coordination for sponsors, committee members, and cross-functional PSI teams, ensuring committee activities are executed efficiently, compliantly, and to the highest quality standards. You will collaborate with global project teams and external experts to support the successful delivery of clinical trials across a variety of therapeutic areas.
You will be responsible for:
Managing the full lifecycle of clinical trial committees, from committee setup and member selection through study conduct and close-out.
Coordinating committee meetings, communications, recommendations, and follow-up activities throughout the course of clinical trials.
Developing, maintaining, and updating committee charters, procedures, and other trial-specific documentation.
Identifying, evaluating, and engaging qualified external committee members based on study requirements, expertise, availability, and independence criteria.
Performing Fair Market Value assessments and preparing honorarium estimates for independent committee members.
Supporting audits and inspections related to committee management activities and contributing to corrective and preventive actions, as needed.
Contributing to the development and continuous improvement of committee-related quality documentation, business processes, templates, and training materials.
Supporting the planning and delivery of internal training on committee management processes.
Qualifications
Bachelor's degree in Life Sciences, Pharmacy, Healthcare, Clinical Research, or a related field.
At least 3 years of experience in clinical research, preferably within a CRO environment.
Experience managing or coordinating clinical trial committees or comparable experience in clinical trial management with exposure to committee processes.
Proven project management and stakeholder coordination skills, with the ability to manage multiple priorities in a fast-paced environment.
Strong organizational, communication, and problem-solving skills with exceptional attention to detail.
Ability to build effective working relationships with sponsors, external experts, and cross-functional teams.
Professional proficiency in English (written and spoken).
Proficiency in Microsoft Office applications and virtual meeting platforms.
Additional Information
Join a collaborative, globally connected team dedicated to ensuring the highest standards of independent clinical trial oversight. In this role, you'll work closely with sponsors, renowned external experts, and cross-functional teams to facilitate unbiased committee governance that supports critical decisions throughout the clinical trial lifecycle.
If you're passionate about clinical research, thrive in a highly organized, stakeholder-facing environment, and enjoy coordinating complex projects that make a real impact on the quality of clinical trials, we'd love to hear from you.
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas.
PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines.
PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world.
PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees.
http://www.psi-cro.com
Offices: Baarerstrasse 113a, Zug, 6300, CH
Number One Patient Enrollment CROClinical ResearchClinical TrialsOncologyHematologyMultiple SclerosisInfectious DiseasesPatient EnrollmentPhase 2Phase 3
How many Science & Research jobs are open in Leuven, Belgium right now?
There are currently 27 open science & research positions in Leuven, Belgium listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Leuven, Belgium?
Companies currently hiring include GlobalFoundries, Materialise, PSI CRO, NuSil Technology, LLC, AECOM, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Leuven, Belgium?
Yes — 9 of the 27 open science & research positions offer remote or hybrid work (0 remote, 9 hybrid).
How do I apply for Science & Research jobs in Leuven, Belgium?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.