Clinical Project Coordinator

2 weeks ago


London, Greater London, United Kingdom Medpace, Inc. Full time

Medpace, Inc. is a leading full-service contract research organization (CRO) offering Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.

About Medpace

We provide a scientific and disciplined approach to accelerate the global development of safe and effective medical therapeutics through our local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

Opportunity Overview

We are currently seeking an Associate Clinical Project Manager to join our London Clinical Trial Management team.

Responsibilities
  • 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
Requirements

To be successful in this role, you will need:

  • A PhD in Life Sciences
  • Fluency in English with solid presentation skills
  • Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
What We Offer

We offer a competitive compensation package, including a salary range of $85,000 - $105,000 per annum, flexible work environment, structured career paths with opportunities for professional growth, company-sponsored employee appreciation events, employee health and wellness initiatives, and much more.



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