Clinical Trial Site Relationship Coordinator (Finnish Speaking)

Overview

In this role you join Medpace’s Clinical Operations team in London to strengthen site networks and drive feasibility for UK and Hungary. You will support pre-award and post-award activities, build strategic site relationships, and help optimize feasibility, site selection, and study start-up. You’ll work with cross-functional teams to understand site capabilities and improve recruitment, retention, and performance. This role offers the chance to shape how we engage sites for successful trials while reducing travel through optimized site relations.

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

• Support ongoing site relationships and identify future business opportunities and feasibilities
• Develop plans for site contact, follow-up, troubleshooting, and coordination of study start-up
• Expedite feasibility activities and support site selection and alignment with studies/therapeutic areas
• Maintain relationships with preferred site networks and oversee master CDAs and meetings with network directors
• Conduct regular site performance reviews and escalate site-related issues throughout study life cycle
• Create and maintain site and country intelligence databases to inform feasibility and recruitment strategies
• Lead process improvement initiatives related to feasibility activities and serve as main contact for project teams on site performance updates
• Support site qualification visits and preparation for site audits as needed

Key requirements

• Bachelor of Science in health-related field
• Minimum 1 year site and clinical trials experience (more for senior roles)
• CRA experience is an asset
• Knowledge of drug development, clinical trial management, and GCP guidelines preferred
• Knowledge of medical terminology and clinical patient management preferred
• Fluency in English; Finnish language is a plus
• Strong organizational and prioritization skills
• Excellent oral and written communication skills
• Proficient in Microsoft Office applications

• organizational skills
• prioritization
• excellent communication
• GCP guidelines familiarity
• clinical trial management
• site liaison and relationship management

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