Associate Clinical Trial Manager (PhD) - Radiopharmaceuticals

Medpace; Stirling; On-site; GBP 30,000 - 45,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits package

Professional growth opportunities

Employee health and wellness initiatives

Job summary

Medpace is looking for a full-time Associate Clinical Trial Manager in Stirling, UK. This role is suitable for candidates with a PhD in Life Sciences and offers a fantastic entry point into the industry with comprehensive training. Responsibilities include collaborating with project teams, managing study supplies, and reporting on project statuses. Benefits include a flexible work environment and competitive compensation packages, making this a great opportunity for recent graduates seeking a career in clinical trial management.

Qualifications

• PhD required in a relevant field.
• Fluency in English with solid presentation skills.
• Ability to work in a dynamic international team.

Responsibilities

• Communicate and collaborate on global study activities.
• Ensure timely and accurate delivery of tasks.
• Compile and maintain project-specific status reports.
• Interact with project teams, sponsors, and vendors.
• Provide oversight of regulatory filing systems.
• Manage study supplies and project timelines.
• Coordinate project meetings and produce minutes.

Skills

Fluency in English

Presentation skills

Ability to work in a fast-paced dynamic industry

Analytical skills

Education

PhD in Life Sciences

Job description

Medpace is currently seeking candidates with Radiopharmaceutical or Nuclear Medicine 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. The 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

Benefits

• 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