Study Coordinator

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) partnering with biotechnology and pharmaceutical companies throughout their clinical development journey. Expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions. The Study Coordinator supports clinical trial site activities and coordinates operational tasks for efficient studies compliant with regulations and protocols.

As part of the SRS/FSP team, dedicate efforts to one sponsor, a global pharmaceutical or biotechnology leader in its therapeutic area. Support clinical trial activities at site level and act as point of contact between study teams and sites. Assist with study documentation while ensuring Good Clinical Practice and regulatory compliance.

Track study progress, support resolution of operational issues at site level, and collaborate with CRAs, project teams, and site staff for smooth execution. Join a team valuing collaboration, quality, and making a difference in patients' lives. Core values of Trust, Quality, Passion, Flexibility, and Sustainability shape culture and decisions.

Opportunities for personal and professional growth await in this rewarding environment. TFS began over 30 years ago in Lund, Sweden, as a full-service global CRO. Over 600 professionals deliver tailored services in more than 50 countries across Dermatology, Neuroscience, Oncology, and Ophthalmology.