NHS and University Clinical Trial Professionals - Career Event: Clinical Trial Management - Medpace,

Medpace; London; On-site; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a Clinical Trial Manager to oversee the operations of clinical studies. This role presents an exciting opportunity for professionals transitioning from the NHS or academic settings into the clinical trials industry. You will manage studies in compliance with regulations and lead project teams to ensure successful outcomes. Join a dynamic environment where your expertise will contribute to the development of safe and effective therapeutics. If you're ready to make a difference and advance your career in a global CRO, this opportunity is for you.

Benefits

Flexible work environment

Competitive compensation and benefits

Generous annual leave

Structured career development opportunities

Employee appreciation events

Health and wellness initiatives

Qualifications

• Experience in clinical trials within NHS or university settings.
• Ability to work in a fast-paced, international environment.

Responsibilities

• Manage day-to-day operations of studies for Biotech sponsors.
• Serve as the primary Sponsor contact for operational issues.

Skills

Clinical Trial Management

Presentation Skills

Fluency in English

Knowledge of ICH/GCP

Project Management

Education

Experience in Clinical Trials

Background in Therapeutic Areas

Job description

NHS or University clinical research professional, considering a change to the Industry?

Medpace is hosting a recruitment event tailored for professionals in the NHS or Academic settings (such as Clinical Trial Managers, Junior Doctors, Clinical Research Coordinators, Clinical Research Nurses, Clinical Practitioners) to be considered for the Clinical Trial Manager position at Medpace.

This is an exciting opportunity for individuals looking to transition into the clinical trials industry! Join us at our London Office to hear from former NHS and university-led clinical research professionals who have successfully made the switch to the private industry and learn how you can transform your career at a global CRO.

Details:

1. Location: Central London
2. Date: Thursday, 10th July 2025
3. Application Close Date: Monday, 7th July 2025

This event offers public sector professionals a chance to enter the industry, receive foundational training, work in an international environment, and advance their careers in therapeutics research and development. Attendance is a first step towards future employment with us.

Next Steps:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted to RSVP.

Responsibilities:

Clinical Trial Manager:

• Manage day-to-day operations of studies conducted by Medpace for Biotech sponsors, in accordance with contracts, ICH/GCP, laws, rules, SOPs, and regulations.
• Serve as the primary Sponsor contact for operational issues and study deliverables.
• Maintain in-depth knowledge of the protocol, therapeutic area, and indication.
• Lead internal project teams and oversee study team deliverables.
• Review and contribute to study protocol, database specifications, and final study reports.
• Develop operational project plans specific to each study.
• Implement and manage a risk-based approach to project execution.
• Manage study vendors.
• Supervise site quality, including oversight of Clinical Research Associates and review of CRA trip reports.

Qualifications:

• Experience in clinical trials within NHS and/or university settings (such as Clinical Trial Managers, Junior Doctors, Clinical Research Coordinators, Clinical Research Nurses, Clinical Practitioners).
• Background in key therapeutic areas is advantageous but not mandatory: Oncology, Cardiovascular, Renal/Gastrointestinal, Nuclear Medicine, Hematology, or Radiopharmaceuticals.
• Fluency in English and strong presentation skills.
• Ability to work in a fast-paced, international environment.
• Please include a cover letter with your application.

About Medpace:

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV services to biotech, pharma, and medical device industries. Headquartered in Cincinnati, Ohio, with over 5,000 employees across 40+ countries, we aim to accelerate the development of safe and effective therapeutics.

Why Join Us?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

Our work over the past 30+ years has positively impacted countless lives. Today, we continue to improve the lives of patients worldwide.

Perks:

• Flexible work environment
• Competitive compensation and benefits
• Generous annual leave
• Structured career development opportunities
• Employee appreciation events
• Health and wellness initiatives

Recognition:

• Forbes’ America's Most Successful Midsize Companies (2021-2024)
• CRO Leadership Awards from Life Science Leader magazine

Next Steps:

A Medpace team member will review your qualifications and contact interested candidates with further details.

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