Study Coordinator

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) partnering with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise spans full-service solutions, resourcing, and Functional Service Provider (FSP) models.

About this Role

As part of our SRS / FSP team, you will be dedicated to one of our pharmaceutical partners, supporting the conduct of hospital-based clinical trials in the UK. The Study Coordinator will play a key role in ensuring accurate data entry, query resolution, and smooth site operations across study locations in London, Cambridge, and Cardiff.

This role offers the opportunity to contribute directly to important clinical studies, with a particular focus on oncology and infectious diseases.

Key Responsibilities

• Perform accurate and timely data entry into study systems.
• Manage and resolve data queries in collaboration with site staff and CRAs.
• Support day-to-day study operations, including scheduling patient visits and maintaining documentation.
• Ensure compliance with study protocols, GCP, and site SOPs.
• Act as a liaison between site staff, sponsor, and CRO teams.
• Assist with monitoring visits, audits, and site readiness activities.

Qualifications

Required :

Nice to Have :

What We Offer

About TFS

Our journey began more than 25 years ago in Lund, Sweden. Today, TFS operates in 17 countries across Europe, North America, Asia-Pacific, and the Middle East, delivering tailored clinical development solutions to our partners.

Our core values — Trust, Quality, Flexibility, and Passion — define who we are and guide how we work. They are the foundation of our culture and our success.