Study Coordinator - Freelance
About The Position
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions. The Study Coordinator will act as the main contact for sponsors, patients, and partners, ensuring smooth study execution. As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area. Please, keep in mind that this is a 0.2 FTE role directed at freelance professionals only.
Requirements
- 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
Responsibilities
- Coordinate communication with sponsors, CROs, ethics committees, and vendors
- Manage patient recruitment, scheduling, and engagement
- Organize study documentation, feasibility responses, and investigator meetings
- Oversee monitoring visits, audits, and regulatory compliance
- Track study progress, budgets, and collaborate with finance, legal, and QA teams
Benefits
- Opportunities for personal and professional growth in a rewarding environment
- Join a team that values collaboration, quality, and making a difference in the lives of patients
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What This Job Offers
Career Level
Mid Level
Education Level
Associate degree
