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:
* Previous experience as a Study Coordinator, Research Nurse, or Clinical Research Professional.
* Strong background in hospital-based clinical studies.
* Knowledge of GCP and clinical trial regulations.
* Excellent organizational and communication skills, with strong attention to detail.
* Ability to work independently while collaborating effectively with cross-functional teams.
Nice to Have:
* Experience in oncology and/or infectious disease studies.
* Familiarity with electronic data capture (EDC) systems.
What We Offer
* Competitive compensation and benefits.
* Opportunity to work on impactful studies in a collaborative international environment.
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.
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