About the role
About this role
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.
Clinical Research Associate is responsible for monitoring study sites, ensuring patient safety, data quality, and compliance with GCP, ICH, and regulatory requirements.
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 part-time opportunity directed atFreelance Professionals only.
Key Responsibilities
- Perform on-site and remote monitoring visits
- Ensure protocol compliance, patient safety, and data integrity
- Review CRFs and source data for accuracy
- Verify informed consent procedures are followed
- Manage investigational product accountability
- Write and submit