eClinical Project Manager (London)

Medpace; Greater London; On-site; GBP 45,000 - 65,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Job summary

Medpace is seeking a full-time, office-based eClinical Project Manager to join our Data Management team in Central London. In this essential role, you will manage multiple eClinical/eCOA projects and ensure the accuracy of data reported by patients in clinical trials.

The ideal candidate will possess a Bachelor's degree and have experience in managing eClinical projects. Medpace offers a flexible work environment and a competitive compensation package along with opportunities for professional growth.

Qualifications

• Bachelor’s degree and prior eClinical experience.
• Excellent organisational, prioritisation, and time-management skills.
• Basic knowledge of medical terminology and clinical research methodologies.

Responsibilities

• Manage multiple projects from an eClinical/eCOA perspective.
• Develop and review study documentation for clinical trials.
• Coordinate overall eClinical activities with sponsors.
• Monitor study timelines in relation to clinical trial needs.
• Attend face-to-face sponsor meetings and investigator meetings.

Skills

Organisational skills

Time-management skills

Knowledge of medical terminology

Experience with eClinical/eCOA projects

Knowledge of technology trends

Education

Bachelor’s degree

Job description

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 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.

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, prioritisation, and time‑management skills.
• Basic knowledge of medical terminology, scientific investigative methodologies, and clinical research methodologies.

Benefits

• 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