Clinical Trial Management Specialist

2 days ago


London, Greater London, United Kingdom Medpace Full time
About the Role

We are seeking an experienced Clinical Trial Management Specialist to join our team. The successful candidate will be responsible for managing clinical trials from start to finish, ensuring timely delivery and high accuracy.

About Medpace

MEDpace is a full-service contract research organization (CRO) providing 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.

Key Responsibilities
  • Manage and coordinate clinical trial activities, ensuring timely delivery and high quality.
  • Collaborate with project coordinators and clinical trial managers to achieve project goals.
  • Compile and maintain project-specific status reports within the clinical trial management system.
Requirements
  • 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.
  • Structured career paths with opportunities for professional growth.

The estimated salary for this role is $80,000 - $110,000 per year, depending on experience.



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