Clinical Trials Site Relations Lead

Medpace; Greater London; On-site; GBP 32,000 - 42,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation package

Competitive PTO

Structured career paths

Employee wellness initiative

Job summary

Medpace is seeking a Clinical Trial Site Relationship Coordinator in London to join our Clinical Operations team. You will help with pre-award and post-award feasibilities, build strategic site relationships, and develop strategies to conduct feasibilities in the UK and Hungary.

Prior clinical research experience or CRA background is welcome. The role focuses on reducing travel while supporting site performance and study setup.

Qualifications

• Bachelor of Science in health-related field.
• 1+ years' site and clinical trials experience.
• CRA experience is an asset.
• Fluency in English; Polish.

Responsibilities

• Provide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments.
• Develop effective plans for site contact and follow-up.
• Support management in expediting feasibility, site selection and study start-up.
• May be responsible for other projects and responsibilities as assigned.
• Serve as site relations and excellence partner by providing oversight and building/retaining relationships of assigned sites within assigned country.
• Conducting/expediting feasibility activities (standalone, blinded, initial, ongoing).
• Proactively researching site landscape/intelligence relevant to recruitment and retention.
• Build and maintain relationships with preferred site networks and flagship sites.

Skills

English fluency

Polish

Education

Bachelor of Science in health-related field

Tools

Microsoft Office

Job description

Medpace is seeking a Clinical Trial Site Relationship Coordinator in London to join our Clinical Operations team. You will help with pre-award and post-award feasibilities, build strategic site relationships, and develop strategies to conduct feasibilities in the UK and Hungary.

Prior clinical research experience or CRA background is welcome. The role focuses on reducing travel while supporting site performance and study setup.