Associate Clinical Trial Manager (PhD) - Oncology

Medpace; London; On-site; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a driven Associate Clinical Trial Manager to join their Clinical Trial Management team. This role offers recent PhD graduates a fantastic opportunity to transition into the clinical research field, with comprehensive training and a clear career path. You will be involved in managing clinical trials, ensuring project timelines are met, and collaborating with various stakeholders. This position not only promises professional growth but also allows you to contribute to the development of innovative therapeutics that can change lives. If you're passionate about making a difference in healthcare, this role is for you.

Benefits

Flexible work environment

Competitive compensation and benefits

Competitive PTO packages

Structured career paths

Employee appreciation events

Health and wellness initiatives

Qualifications

• PhD graduates with strong analytical and presentation skills are preferred.
• Ability to work in a fast-paced environment with an international team.

Responsibilities

• Communicate and collaborate on global study activities.
• Compile and maintain project-specific status reports.
• Provide oversight and quality control of regulatory filings.

Skills

Analytical Skills

Presentation Skills

Collaboration

Project Management

Education

PhD in Life Sciences

Job description

Associate Clinical Trial Manager (PhD) - Oncology

Join to apply for the Associate Clinical Trial Manager (PhD) - Oncology role at Medpace

Associate Clinical Trial Manager (PhD) - Oncology

Join to apply for the Associate Clinical Trial Manager (PhD) - Oncology role at Medpace

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 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
  
  

Medpace Overview

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 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.

EO/AA Employer M/F/Disability/Vets

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Pharmaceutical Manufacturing

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