NHS Professionals - Career Event: Clinical Trial Management - Medpace, London

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 daily operations of clinical studies. This role offers a unique opportunity for professionals transitioning from the NHS or academic settings into the dynamic clinical trials industry. Join a forward-thinking organization dedicated to improving lives through impactful research and development. With a focus on career growth, you will lead project teams, manage study vendors, and ensure compliance with regulations. If you're ready to make a difference and accelerate your career in therapeutics research, this opportunity is for you.

Benefits

Flexible work environment

Competitive compensation and benefits

Generous annual leave

Structured career development

Employee appreciation events

Health and wellness programs

Qualifications

• Experience in clinical trials from NHS or university settings.
• Fluency in English with strong presentation skills.

Responsibilities

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

Skills

Clinical Trial Management

Presentation Skills

Fast-paced Environment Adaptability

Education

Degree in Medicine or Life Sciences

Clinical Research Certification

Job description

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

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

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

Location: Central London

Date: Thursday 10th July 2025

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 accelerate their careers in therapeutics research and development. Attending this event is a first step toward securing a position with us.

Next Steps:

A member of our recruitment team will review your qualifications and contact interested candidates for an RSVP.

Responsibilities

Clinical Trial Manager:

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

Qualifications

• Experience in clinical trials from NHS and/or university settings (e.g., Clinical Trial Managers, Junior Doctors, Clinical Research Coordinators, Nurses, Practitioners).
• Background in key therapeutic areas is advantageous but not essential: Oncology, Cardiovascular, Renal/Gastrointestinal, Nuclear Medicine, Hematology, or Radiopharmaceuticals.
• Fluency in English with strong presentation skills.
• Ability to work in a fast-paced, dynamic, and 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 development services to biotech, pharma, and medical device industries. Our mission is to accelerate the development of safe, effective therapeutics worldwide, leveraging local expertise across major therapeutic areas. Headquartered in Cincinnati, Ohio, with over 5,000 employees across 40+ countries.

Why Choose Medpace?

People. Purpose. Passion. Make a difference today and tomorrow. Join us and be part of impactful work that improves lives.

Perks and Recognition

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

Recognized by Forbes as one of America's Most Successful Midsize Companies (2021-2024) and recipient of CRO Leadership Awards for excellence in the industry.

Next Steps

A Medpace team member will review your application and contact suitable candidates for further steps.

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