eClinical Project Manager (London)

Medpace; City Of London; Vor Ort; GBP 60.000 - 90.000; Vollzeit

Benefits dieser Stelle

Competitive compensation

Health and retirement benefits

WFH flexibility after training

Company-sponsored events

Zusammenfassung

Medpace, Inc. is seeking a full-time, office-based eClinical 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.

Qualifikationen

• Bachelor’s degree with eClinical experience, including setting up and managing multiple eClinical/eCOA projects and acting as the main point of contact for the sponsor.
• General knowledge of technology trends and system / application development.
• Exellent organisational, prioritization, and time management skills.
• Basic medical terminology knowledge and understanding of clinical research methodologies.

Aufgaben

• Manage multiple eClinical/eCOA projects from start to finish.
• Develop and review study documentation related to eClinical/eCOA activities for clinical trials with sponsor companies and other departments.
• Coordinate overall eClinical activities by serving as primary contact for the sponsor.
• Monitor study timelines in relation to clinical trial needs.
• Attend sponsor and Investigator Meetings.

Kenntnisse

eClinical

eCOA

Project management

Sponsor liaison

Ausbildung

Bachelor’s degree

Jobbeschreibung

Job Summary

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based eClinical Project Manager to join our Data Management team in Central London. The eClinical Project Manager role at Medpace is a crucial component of the clinical trial process. This role will work with both local and international teams and will manage global studies, ensuring the accuracy of data reported by patients for clinical studies. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• Manage multiple projects from am eClinical/eCOA perspective;
• Develop and review study documentation related to eClinical/eCOA activities for clinical trials with sponsor companies and other departments;
• Coordinate overall eClinical activities by serving as primary contact for the sponsor;
• Monitor study timelines in relation to clinical trial needs;
• Attend face to face sponsor meetings and Investigator Meetings

Qualifications

• Bachelor’s degree and prior eClinical experience; including setting up and managing multiple eClinical/eCOA projects and acting as the main point of contact for the sponsor;
• General knowledge of technology trends and system / application development;
• Possess excellent organisational, prioritization, and time management skills;
• A basic knowledge of medical terminology is needed, as well as knowledge of a scientific investigative methodologies and clinical research methodologies.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
  • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• • Office based environment with on-site mentors
  • Defined career paths with clear advancement opportunities
  • Industry renowned onboarding and training programs designed to accelerate professional development
  • Ongoing training and continuous learning opportunities throughout your career
  • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• • Competitive compensation programs that recognize and reward performance
  • Comprehensive health, wellness, retirement, and PTO benefits
  • Office based culture with occasional WFH that provides flexibility for eligible positions after training
  • Company-sponsored social events

Please note benefits may vary based on country.