Clinical Research Coordinator

1 day ago


London, Greater London, United Kingdom Medpace Full time
Company Overview

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

About the Role

We are seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager position to join our Clinical Trial Management team. The successful candidate will work closely with project coordinators and clinical trial managers to ensure timely delivery of recurrent tasks consistently with a high degree of accuracy.

Responsibilities
  • Communicate and collaborate on global study activities
  • 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 internal project teams, sponsors, study sites, and third-party vendors
  • Manage and perform quality control of internal regulatory filing systems
  • 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
Salary and Benefits

We offer a competitive salary range of $80,000 - $110,000 per annum, plus benefits including flexible work environment, competitive compensation package, PTO packages, structured career paths, company-sponsored employee appreciation events, and employee health and wellness initiatives.



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