Senior Clinical Project Manager

Richmond Pharmacology; London; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading Clinical Research Organisation in central London is seeking a Senior Clinical Project Manager to oversee clinical trials from setup to post-clinical phases. The role involves managing cross-functional teams, ensuring compliance with protocols and regulations, and delivering projects within budget. Ideal candidates will have a strong background in project management and excellent communication skills.

Benefits

Private Medical

Private Dental

Pension

25 days Annual leave plus bank holidays

Qualifications

• Previous experience in Clinical Project Management.
• Professional communication skills with external clients and internal teams.

Responsibilities

• Manage and coordinate the setup and execution of clinical trials.
• Serve as the primary contact for sponsors and project teams.
• Supervise and mentor Clinical Research Specialists and Clinical Project Managers.

Skills

Communication

Project Management

Education

BSc in Life Sciences

MSc or Postgraduate Diploma

Job description

Job Title: Senior Clinical Project Manager

Location: London Bridge, SE1

Term: Permanent, Full-time

Salary: Competitive + Benefits (Private Medical, Private Dental, Pension, 25 days Annual leave plus bank holidays & Many more)

Richmond Pharmacology is an early phase Clinical Research Organisation (CRO) conducting pioneering trials with healthy participants and patients. Our experienced, world-renowned team, central London location, and global reach make Richmond Pharmacology an exciting and dynamic workplace.

Purpose of the Job:

The Senior Clinical Project Manager oversees the entire trial process from setup to post-clinical phases, managing operational delivery. This role involves coordinating cross-functional teams, liaising with internal departments and external stakeholders to ensure high-quality trial outputs. The manager is responsible for delivering projects within budget, adhering to company and regulatory standards, and complying with protocols, SOPs, GCP, and local regulations.

Main Duties and Responsibilities:

1. Manage and coordinate the setup and execution of clinical trials according to protocols, SOPs, GCP, and relevant guidelines.
2. Serve as the primary contact for sponsors, vendors, and project teams.
3. Assist with trial design by collaborating with sponsors and Principal Investigators, evaluating information critically, and making informed decisions regarding study design and timelines.
4. Perform quality checks and coordinate the flow of study documents before study initiation.
5. Review meeting agendas, minutes, documents, and schedules.
6. Coordinate external and internal study meetings as needed.
7. Supervise and mentor Clinical Research Specialists (CRS) and Clinical Project Managers (CPMs).
8. Maintain and ensure quality control of the Investigator Site File.
9. Oversee effective trial close-out activities.
10. Manage data query resolutions to facilitate timely database lock and study report reviews for regulatory submission.
11. Engage in continuous improvement activities to enhance processes and workplace culture.

Skills and Experience:

1. BSc in Life Sciences or equivalent; MSc or Postgraduate Diploma preferred.
2. Previous experience in Clinical Project Management.
3. Professional communication skills with external clients and internal teams.
4. Excellent written and verbal communication skills.
5. Strong knowledge of project management methodologies and practical application.

Application:

If interested, please submit your CV and registration details. Note that due to high application volume, responses may be delayed. We appreciate your patience and understanding.