eClinical Coordinator (London)

Overview

As an eClinical Coordinator in Medpace’s Data Management team, you help ensure accurate patient data across clinical studies. You will work with the eClinical Project Manager and cross-functional partners to support trial data integrity and reporting. Your role includes configuring and testing applications, coordinating with vendors, and producing study metrics. This position offers a structured onboarding and opportunities to grow within a mission-driven CRO. You’ll contribute to impactful trials in a collaborative, growth-focused environment.

Pay / 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

Responsibilities

• Collaborate on project teams across studies
• Coordinate with vendors to ensure electronic form compliance
• Partner with Sponsors to define study-specific application requirements
• Create and maintain metric reports and study documents
• Assist Clinical DB Programmers with application configuration and testing
• Troubleshoot application issues with sites and Sponsors
• Report compliance metrics to Sponsors

Key requirements

• Bachelor in Life Sciences
• strong attention to detail
• excellent Microsoft Excel and Word skills
• clear oral and written English communication
• 1-2 years of pharma or CRO experience (preferred)

• attention to detail
• clear communication
• team collaboration
• Microsoft Excel
• Microsoft Word
• data reporting

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