Associate Clinical Trial Manager - Oncology / Radiopharmaceuticals / Renal / Cardiovascular

TN United Kingdom; Stirling; On-site; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a dedicated Associate Clinical Trial Manager to join their innovative team in Stirling. This full-time role offers an exciting opportunity for recent PhD graduates to enter the dynamic field of clinical trial management, focusing on cutting-edge radiopharmaceuticals. You will collaborate with global teams, ensuring the accuracy and timely delivery of clinical trial activities. With a strong emphasis on professional growth, this position provides comprehensive training and a structured career path in a supportive environment. Join a company that is making a significant difference in the medical field and take your career to new heights.

Benefits

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Qualifications

• PhD or Post-Doc in nuclear medicine or related field required.
• Fluency in English with solid presentation skills necessary.

Responsibilities

• Communicate and collaborate on global study activities.
• Ensure timely delivery of project-specific tasks with high accuracy.

Skills

Analytical Skills

Presentation Skills

Collaboration

Project Management

Education

PhD in Radiopharmaceuticals

Post-Doctoral Research

Job description

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Associate Clinical Trial Manager - Oncology / Radiopharmaceuticals / Renal / Cardiovascular, Stirling

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Client:

Location:

Stirling, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

31f5346a1690

Job Views:

5

Posted:

05.05.2025

Expiry Date:

19.06.2025

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Job Description:

Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging / radiopharmaceuticals or / radiation oncology for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work 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 radiopharmaceuticals (molecular radiotherapy, radiotheranostics, targeted radionuclide therapy). 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 or Post-Doc related to Radiopharmaceuticals ( nuclear medicine/medical physics/medical imaging/ radiation oncology or related )
• 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 organisation (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 5,000 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 2024
• Continually 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.

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