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Associate Clinical Trial Manager (PhD) - Gastrointestinal

Medpace, City of London

Associate Clinical Trial Manager (PhD) - Gastrointestinal

Salary not available. View on company website.

Medpace, City of London

  • Full time
  • Permanent
  • Onsite working

Posted today, 30 Sep | Get your application in now to be one of the first to apply.

Closing date: Closing date not specified

Job ref: 66f10fbe2719421abe98d606d310e94e

Location ref: City of London

Full Job Description

Associate Clinical Trial Manager (PhD) - Gastrointestinal


Location: City of London, Greater London, GB, EC4N 6JD


Application Deadline: 2026-09-26


Post Date: 2026-12-27T15:01:06.767


Job Summary


Medpace is currently seeking candidates with Gastrointestinal related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our 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 PhD graduates to enter the industry, 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).


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

  • 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 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


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Job Summary Medpace is currently seeking candidates with Gastrointestinal related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our 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 PhD graduates to enter the industry, 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). 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 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 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 #J-18808-Ljbffr

Direct job link

https://www.jobs24.co.uk/job/associate-clinical-trial-manager-phd-gastrointestinal-127484385
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