Associate Clinical Trial Manager (PhD) - Cardiovascular

Medpace; Greater London; On-site; GBP 40,000 - 60,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits package

Structured career paths

Employee health and wellness initiatives

Job summary

Medpace is seeking an Associate Clinical Trial Manager (aCTM) in London to join their Clinical Trial Management team. This full-time position is ideal for recent PhD graduates in Life Sciences looking to enter the industry with a focus on clinical project management.

The role offers comprehensive training, competitive compensation, and opportunities for career advancement. Applicants should demonstrate strong analytical skills and the ability to thrive in a collaborative international environment.

Qualifications

• PhD in Life Sciences is required for the role.
• Fluent English with solid presentation skills necessary.
• Ability to work in an international team and dynamic environment.
• Previous experience in CRO or pharmaceutical industry is advantageous but not necessary.

Responsibilities

• Communicate and collaborate on global study activities with the project team.
• Ensure timely delivery of tasks with high accuracy.
• Compile and maintain project-specific status reports.
• Interact with project team, sponsor, and study sites.
• Provide oversight of internal regulatory filing.
• Manage study supplies and create project timelines.
• Coordinate project meetings and produce minutes.

Skills

Fluency in English

Analytical skills

Presentation skills

Ability to work in a fast-paced dynamic environment

Education

PhD in Life Sciences

Job description

Medpace is currently seeking candidates with Cardiovascular related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London 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

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

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.