Eclinical Coordinator - Trials Data & Support

Medpace; Greater London; On-site; GBP 30,000 - 45,000; 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 is seeking a full-time, office-based eClinical Coordinator to join its Data Management team in Central London. The role focuses on ensuring accurate data reported by patients for clinical studies, working with the eClinical Project Manager and sponsors.

Onboarding provides training to build expertise in this clinical trial environment, with opportunities to grow within a leading CRO and develop strong data management and communication skills.

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

Microsoft Excel

Microsoft Word

English communication

Education

Bachelor's degree in Life Sciences or Mathematics

Job description

Medpace is seeking a full-time, office-based eClinical Coordinator to join its Data Management team in Central London. The role focuses on ensuring accurate data reported by patients for clinical studies, working with the eClinical Project Manager and sponsors.

Onboarding provides training to build expertise in this clinical trial environment, with opportunities to grow within a leading CRO and develop strong data management and communication skills.