TFS HealthScience
Location
San Diego, California
The Study Coordinator serves as the primary contact for sponsors, patients, and partners to ensure smooth study execution. Key duties include managing patient recruitment, coordinating communication with ethics committees, and overseeing regulatory compliance and audits.
Candidates need at least 2 years of experience in clinical research or healthcare, with a background as a Study Coordinator, Nurse, or a life sciences degree. Proficiency in English, MS Office, and knowledge of ICH-GCP and clinical trial processes are required.
2+ years of experience in clinical research or healthcare Background as Study Coordinator/Nurse or a life sciences degree Knowledge of ICH-GCP, AMG, and clinical trial processes Strong organization, communication, and independent working skills Fluent in English and proficient in MS Office
We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients. Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to excellence. Together, we make a difference. A Bit More About Us Our journey began over 30 years ago in Sweden, in the city of Lund. As a full-service global CRO, we build solution-driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.
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