Clinical Project Manager

TN United Kingdom; London; Remote; GBP 50,000 - 90,000; Full time

Job summary

An established industry player is seeking a Clinical Project Manager to oversee clinical research trials. This fully remote, full-time role involves planning, managing timelines, and ensuring compliance with regulatory standards. The ideal candidate will have a strong background in clinical trial management and possess excellent communication skills. Join a diverse and inclusive workplace that values your contributions and fosters personal growth. If you're passionate about advancing healthcare and driving successful studies, this opportunity is perfect for you.

Qualifications

• Bachelor's or advanced degree required.
• Several years of clinical trial experience needed.

Responsibilities

• Plan and manage clinical studies from start to finish.
• Ensure compliance with FDA and ICH-GCP regulations.
• Monitor project budgets and timelines.

Skills

Clinical Trial Management

Regulatory Compliance

Risk Assessment

Project Management

Communication Skills

Education

Bachelor's Degree

Master's Degree

PhD

Job description

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About ProPharma

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, medical device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest Research Consulting Organization (RCO), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Position: Clinical Project Manager

We are seeking a Clinical Project Manager to support ProPharma by providing strategic and tactical operational planning and execution for upcoming studies. The role involves oversight and conduct of clinical research trials, ensuring compliance with applicable regulations and that the quality of clinical data meets regulatory authority standards.

This is a fully remote, full-time, permanent position.

Key Responsibilities

1. Plan and manage assigned studies from start to closeout.
2. Manage project timelines and budgets.
3. Proactively identify concerns, issues, and delays.
4. Develop risk assessments and contingency plans.
5. Coordinate risk mitigation across functional areas.
6. Serve as the primary communication link for the clinical project team and stakeholders.
7. Participate in project kick-off meetings.
8. Provide regular updates to clients and facilitate communication.
9. Monitor project budgets and ensure margins are maintained.
10. Provide study-specific training for clinical staff.
11. Assess and monitor resourcing needs throughout the study lifecycle.
12. Develop, analyze, and report study metrics, communicating risks proactively.
13. Create and maintain Study Project Plans.
14. Contribute strategic input to study documents.
15. Manage study drug and non-drug supplies.
16. Plan and execute Investigator Meetings.
17. Develop and present training materials for various audiences.
18. Assist in vendor selection and contracting.
19. Ensure compliance with FDA, ex-US regulations, ICH-GCPs, and SOPs.
20. Develop subject recruitment and retention strategies.
21. Oversee TMF maintenance and quality review.

Qualifications

• Bachelor’s or advanced degree (e.g., Master, PharmD, PhD) or equivalent experience.
• Several years of clinical trial and research experience.
• Knowledge of FDA and/or ex-US regulations, ICH guidelines, and GCPs.
• Experience managing and mentoring junior staff.
• Experience with change management initiatives.

We value diversity and strive to create an inclusive workplace where everyone can be their authentic self. We are committed to diversity, equity, and inclusion, fostering a safe environment that empowers all employees to succeed.

***ProPharma Group does not accept unsolicited resumes from recruiters or third parties. Please do not contact anyone regarding this posting.***