At a Glance
- Tasks: Manage clinical trial committees and ensure efficient execution of activities.
- Company: Global CRO with over 30 years of experience in clinical research.
- Benefits: Collaborative environment, career growth, and the chance to impact global healthcare.
- Other info: Join a globally connected team dedicated to high standards in clinical trial oversight.
- Why this job: Be at the forefront of clinical trials and make a real difference in healthcare.
- Qualifications: Bachelor's degree in Life Sciences and 3 years of clinical research experience.
The predicted salary is between 45000 - 55000 £ per year.
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.
- Summary
- Type: Full-time
- Function: Other Experience level: Mid-Senior Level
- Industry: Pharmaceuticals
Trial Committee Manager employer: PSI CRO
As a Remote Director of Business Development at our company, you will join a supportive and innovative team that prioritises employee well-being and professional growth. With a strong emphasis on collaboration and a commitment to making a difference in medical science, we offer a dynamic work culture, competitive benefits, and opportunities for career advancement, all while working from the comfort of your own home in the UK.
StudySmarter Expert Advice🤫
We think this is how you could land Trial Committee Manager
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like PSI CRO.
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When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what PSI CRO is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Trial Committee Manager
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at PSI CRO!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show PSI CRO that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at PSI CRO!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At PSI CRO, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at PSI CRO
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at PSI CRO that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with PSI CRO’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
