At a Glance
- Tasks: Join our team to manage clinical trials and collaborate on global study activities.
- Company: Medpace, a leading company in clinical trial management with a supportive culture.
- Benefits: Flexible work environment, competitive pay, and structured career growth opportunities.
- Other info: Exciting opportunity for recent graduates to transition from academia to industry.
- Why this job: Kickstart your career in the clinical trials industry with hands-on training and real impact.
- Qualifications: PhD in Life Sciences and strong communication skills required.
The predicted salary is between 30000 - 40000 £ per year.
Medpace is delighted to host a Recruitment Event tailored to candidates studying or holding a PhD in Life Science. This is a rare and exciting opportunity for individuals seeking to make a switch from academia to the Clinical Trials Industry!
LOCATION: Central London
DATE: Thursday 6th August 2026
APPLICATION CLOSE DATE: Monday 3rd August 2026
At this event, Medpace is seeking to meet candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) role to join our global Clinical Operations team. The aCTM will be working closely with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidates must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and accelerate 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).
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:
- PhD in Life Sciences
- A background in one of our key therapeutic focus areas is of advantage, but not a must: Oncology, Cardiovascular, Endocrine/Metabolic, Nuclear Medicine, or Radiopharmaceuticals
- Fluency in English with solid presentation skills
- Ability to work in a fast-paced dynamic industry within an international team
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 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
PhD Career Event: Clinical Trial Management – Medpace London employer: Medpace, Inc.
Medpace is an exceptional employer, offering a dynamic and supportive work environment in the heart of Central London. With a strong focus on employee growth, we provide structured career paths, competitive compensation, and comprehensive benefits, ensuring that our team members thrive both personally and professionally. Join us to be part of a globally recognised company that values innovation and collaboration in the clinical trials industry.
