Global eClinical PM – Lead Multi-Study Trials (Hybrid) in London

Global eClinical PM – Lead Multi-Study Trials (Hybrid) in London

London Full-Time 45000 - 55000 Β£ / year (est.) Hybrid
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At a Glance

  • Tasks: Lead global clinical studies and ensure accurate patient data reporting.
  • Company: Join Medpace, a fast-growing CRO with a dynamic team in Central London.
  • Benefits: Enjoy a competitive salary, career development, and a hybrid work model.
  • Other info: Great opportunities for career growth in a supportive environment.
  • Why this job: Make a real impact in healthcare while collaborating with international teams.
  • Qualifications: Experience in project management and strong communication skills required.

The predicted salary is between 45000 - 55000 Β£ per year.

Medpace, Inc. is seeking a full-time, office-based e Clinical Project Manager to join our Data Management team in Central London.

You will oversee global studies and ensure accurate data reported by patients for clinical studies, collaborating with local and international teams.

The role emphasizes managing sponsor relationships, timelines, and study documentation, with opportunities to develop your career within a fast-growing CRO.

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Global eClinical PM – Lead Multi-Study Trials (Hybrid) in London employer: Medpace

Medpace is an exceptional employer, offering a collaborative and purpose-driven work environment in Cincinnati, Ohio, where employees can thrive alongside industry-leading experts in clinical research. With a strong focus on continuous learning and professional development, Medpace provides defined career paths, comprehensive benefits, and a culture that encourages innovation and employee contributions. Join us to make a meaningful impact on global health while enjoying competitive compensation and a supportive office-based atmosphere.

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Contact Details:

Medpace Recruitment Team

We think you need these skills to ace Global eClinical PM – Lead Multi-Study Trials (Hybrid) in London

Project Management
Data Management
Clinical Study Oversight
Sponsor Relationship Management
Timeline Management
Study Documentation
Collaboration Skills