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Medspace

PhD Career Event: Clinical Trial Management – Medpace London

PhD Career Event: Clinical Trial Management – Medpace London

Posted 3 weeks ago

LondonOn-Site

PhD Career Event: Clinical Trial Management – Medpace London

Medspace

Permanent
Full-Time
Sign up to unlock the estimation.Sign up to unlock the estimation~£36,000 - £60,000per annum· Meev estimate

Posted 3 weeks ago

Description

Location: Central London
Date: Thursday 6th August 2026
Application Close Date: Monday 3rd August 2026

Associate Clinical Trial Manager
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. Candidate 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 is an equal opportunity employer.
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Medspace

A scientifically driven global CRO accelerating clinical development for biotech and pharma.

CincinnatiContract Research1000+
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Medspace

Contract Research

Shape the future of medicine by embedding deep scientific expertise into the most innovative clinical trials. Work alongside cross functional experts who turn complexity into clarity, trusted by biotech to accelerate treatments that matter.

Click to learn more
Medspace logo

Medspace

Contract Research

Shape the future of medicine by embedding deep scientific expertise into the most innovative clinical trials. Work alongside cross functional experts who turn complexity into clarity, trusted by biotech to accelerate treatments that matter.

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