Associate Clinical Trial Manager - Radiopharmaceuticals

Medpace; Greater London; On-site; GBP 35,000 - 45,000; Full time

Job summary

A leading clinical research organization is seeking a full-time Associate Clinical Trial Manager to join their Clinical Trial Management team in Greater London. Ideal for recent PhD graduates, this role offers the chance to develop skills in clinical project administration and management in an international environment, with comprehensive training and a focus on radiopharmaceuticals.

Benefits

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths

Employee health and wellness initiatives

Qualifications

• PhD or Post-Doc in Radiopharmaceuticals or related field.
• Fluency in English with solid presentation skills.
• Ability to work within an international team.

Responsibilities

• Communicate on global study activities with team members.
• Ensure timely delivery of tasks with high accuracy.
• Compile project-specific status reports within the system.
• Interact with internal project teams and external partners.
• Oversee internal regulatory filing system.
• Create and maintain project timelines.

Skills

PhD in Radiopharmaceuticals

Fluency in English

Ability to work in a fast-paced environment

Education

PhD or Post-Doc related to Radiopharmaceuticals

Job description

Overview

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
• 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

Qualifications

• PhD or Post-Doc in 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, international environment
• Experience in CRO or pharmaceutical industry is beneficial but not required

Why Medpace

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.

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