Trial Committee Manager

Role Summary

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.

Requirements

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.
• 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.

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 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.

About the Company

Why Join PSI?

At PSI, we believe exceptional people deserve an exceptional workplace.

When you join PSI, you'll benefit from

A stable, privately held CRO that has never undergone a merger or acquisition and has never experienced company-wide layoffs.

A unique leadership-focused CRA role with minimal travel and little to no routine site assignments.

Opportunities to mentor other CRAs and expand your leadership skills.

A collaborative, people-first culture where employees are genuinely supported.

Career development opportunities across a growing global organization.

The chance to contribute to innovative clinical research that improves patients' lives.

We are the company that cares - for our staff, our clients, our partners, and the quality of the work we do.

Founded in 1995, PSI CRO is a privately owned, global Contract Research Organization with more than 3,000 employees dedicated to advancing medical science and bringing new therapies to patients worldwide.

In an industry shaped by mergers, acquisitions, and restructures, PSI stands apart. We have remained privately held, have never undergone a merger or acquisition, and have never experienced company-wide layoffs. Our long-term stability allows us to invest in our people, foster meaningful careers, and build lasting partnerships with our clients.

If you're looking for a collaborative organization where you can continue to grow while making a meaningful impact, PSI is the right place for you.