Medical Doctor / MBBS Career Event: Clinical Trial Management – Medpace London

Medpace is delighted to host a Recruitment Event tailored to candidates with a Bachelor of Medicine, Bachelor of Surgery qualification.

This is a rare and exciting opportunity for Medical Doctors to make a switch to the Clinical Trials Industry!LOCATION: Central LondonDATE: Thursday 30th July 2026APPLICATION CLOSE DATE: Monday 27th July 2026Associate Clinical Trial ManagerMedpace is currently seeking candidates with Bachelor of Medicine, Bachelor of Surgery qualification for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team.

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities.

Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.A fantastic opportunity for recent junior doctors to enter the clinical research industry in an operations role, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics.

Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

What to Expect Next:A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an RSVP.

Responsibilities

• Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
• Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
• Compile and maintain project-specific status reports within the clinical trial management system
• Interact with the internal project team, Sponsor, study sites, and third-party vendors
• Provide oversight and quality control of our internal regulatory filing system
• Provide oversight and management of study supplies
• Create and maintain project timelines
• Coordinate project meetings and produce quality minutes

Qualifications

• Bachelor of Medicine, Bachelor of Surgery
• Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team
• Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
• Medpace

Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.

We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow.

Join Us

Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace

Perks

• Flexible work environment Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events Employee health and wellness initiatives
• Awards
• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
• What To Expect Next
• A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.