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About this role
TFS HealthScience is a leading global midsize Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes fullservice capabilities resourcing and Functional Service (FSP) solutions.
The Site Coordinator is responsible for supporting investigational site operations to ensure clinical studies are conducted efficiently and with highquality standards. You will work under the supervision of the Principal Investigator contributing to patient recruitment data entry and overall study execution.
As part of our SRS/FSP team you will be dedicated to one sponsor a global pharmaceutical/biotech company that is an industry leader in clinical research and drug development.
We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. Youll be joining a team that values collaboration innovation and making a difference in the lives of patients.
Our journey began over 27 years ago in Sweden in the city of Lund. As a fullservice global Contract Research Organization (CRO) we build solutiondriven teams working towards a healthier future. Bringing together over 800 professionals TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology Neuroscience Oncology and Ophthalmology.
Our core values of Trust Quality Passion Flexibility and Sustainability guide us in attracting and retaining valuable talent. These values foster high employee engagement and satisfaction ensuring we cultivate a collaborative culture that drives innovation and excellence. Together we make a difference.
Apply now to be part of our mission to build a healthier future!
Full Time