Impactful eClinical Data Coordinator (London)

Medpace; Greater London; On-site; GBP 32,000 - 46,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits

Competitive PTO packages

Structured career paths with growth

Company-sponsored employee events

Employee health and wellness

Awards

Job summary

Medpace in Central London is seeking a full-time, office-based eClinical Coordinator to join our Data Management team. The role works with the eClinical Project Manager to ensure the accuracy of data reported by patients for clinical studies, supporting the clinical trial process.

You will participate in onboarding, work with vendors, develop study-specific requirements, create and maintain metric reports, assist in configuring applications, and troubleshoot issues with sites and sponsors.

Qualifications

• Bachelor's degree in Life Sciences or Mathematics.
• Strong attention to detail.
• Excellent working knowledge of Microsoft Excel and Word.
• Solid oral and written English language communication skills.
• Training is available for entry-level candidates.

Responsibilities

• Participate as part of a team on various project(s).
• Work with vendors to ensure patient forms meet their respective electronic requirements.
• Partner with Sponsors to develop application requirements for each unique study.
• Assist in the creation and maintenance of metric reports and study specific documents.
• Assist Clinical Db Programmers with configuring and testing applications.
• Troubleshoot issues with applications by working with sites/sponsors.
• Report compliance metrics to Sponsors.

Skills

Attention to detail

English communication

Education

Bachelor's degree in Life Sciences or Mathematics

Tools

Excel

Word

Job description

Medpace in Central London is seeking a full-time, office-based eClinical Coordinator to join our Data Management team. The role works with the eClinical Project Manager to ensure the accuracy of data reported by patients for clinical studies, supporting the clinical trial process.

You will participate in onboarding, work with vendors, develop study-specific requirements, create and maintain metric reports, assist in configuring applications, and troubleshoot issues with sites and sponsors.