Eclinical Project Manager (London)

Medpace; Greater London; On-site; GBP 60,000 - 90,000; Full time

Job summary

Medpace in Central London is seeking a full-time, office-based eClinical Project Manager to join our Data Management team. The role manages global studies, ensuring data accuracy reported by patients for clinical trials, and works with local and international teams.

You will coordinate eClinical/eCOA activities, develop study documentation, and monitor timelines. The position offers a dynamic environment with opportunities for professional growth within a leading CRO.

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.
• Excellent organisational, prioritization, and time management skills.
• Basic knowledge of medical terminology and scientific/clinical research methodologies.

Responsibilities

• Manage multiple projects from an 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

Skills

eClinical experience

Technology trends knowledge

Organisational skills

Time management

Medical terminology knowledge

Education

Bachelor's degree

Job description

eClinical Project Manager (London)

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). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Awards

Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024. Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.