Associate Clinical Trial Manager (PhD) - Gastrointestinal

Medpace; Greater London; On-site; GBP 60,000 - 80,000; Full time

Job summary

A clinical contract research organization in Greater London is seeking an office-based Associate Clinical Trial Manager (aCTM) with a PhD in Life Sciences. This position offers an opportunity for recent graduates to enter the industry, receive foundational training, and develop a career in clinical trial management. Candidates will engage in global study activities, maintain project timelines, and ensure quality control of regulatory filings. A flexible work environment and competitive compensation are part of the perks.

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

• Candidates should expect an intensive training period.
• Ability to work in an international team is essential.
• Prior experience in CRO or pharmaceutical industry is advantageous.

Responsibilities

• Communicate and collaborate on global study activities.
• Ensure timely delivery of tasks with high accuracy.
• Compile and maintain project-specific status reports.
• Provide oversight and quality control of regulatory filing.
• Create and maintain project timelines.
• Coordinate project meetings and produce minutes.

Skills

Fluency in English

Presentation skills

Ability to work in a fast-paced dynamic industry

Education

PhD in Life Sciences

Job description

Overview

Medpace is currently seeking candidates with 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 part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. The position offers an opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop a career in the research and development of cutting-edge therapeutics. Candidates should expect an intensive training period and the aptitude for an accelerated career path into Clinical Trial Management (CTM).

Responsibilities

• Communicate and collaborate on global study activities; work closely with the project coordinator and clinical trial manager
• Ensure timely delivery of recurrent tasks 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

About Medpace

Medpace is a full-service clinical contract research organization (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 a 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, Medpace employs more than 5,000 people across 40+ countries.

Perks & 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

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