Clinical Trial Site Relationship Coordinator (Finnish Speaking)

Our clinical activities are growing rapidly, and we are seeking a full-time Clinical Trial Site Relationship Coordinator to join our Clinical Operations team in London. This role involves pre-award and post-award study feasibilities, building and maintaining strategic relationships with our network of sites, and developing strategies to conduct feasibilities in the UK and Hungary. The position may suit someone with previous clinical research experience or a CRA looking to reduce travel.

If you want an exciting career within a company that excels in delivering innovative research and development of cutting-edge drugs, where you can grow your potential, this is the opportunity for you.

• 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 the assigned country.
• Conduct/expedite feasibility activities (standalone, blinded, initial, ongoing), supporting management with site selection/alignment with studies and/or therapeutic areas, and study start-up.
• Proactively research and understand specified site landscape/intelligence (KOL presence and knowledge, site capabilities, country standard of care and medical practices, etc.) as it relates to specific patient population, recruitment, and retention.
• Build and maintain relationships with preferred site networks/flagship sites, including facilitating master CDAs and holding meetings with network directors.
• Conduct regular performance reviews for sites participating in our studies, ensuring quality study delivery.
• Serve as an escalation point for site-related issues throughout the life cycle of a study.
• Provide ongoing support of sites, including identifying and discussing future new business.
• Develop effective plans for site contacts, troubleshooting, and follow-up.
• Develop an intelligence database with site and country intelligence.
• Support management with process improvement initiatives regarding feasibility activities.
• Serve as main point of contact for project teams regarding site performance issues and updates on pertinent site information.
• May be responsible for other projects and responsibilities as assigned, including site Qualification Visits and prep/consultation support for site audits.

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

At Medpace, you will find work that is both challenging and rewarding. You will be given the tools and training to succeed, and you will be rewarded for strong performance with opportunities to grow professionally.

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach.

Flexible work environment, competitive compensation and benefits package, competitive PTO packages, structured career paths with opportunities for professional growth, and employee health and wellness initiatives.