- Buffalo, New York, United States +1 more
- Full-time · Entry
- 2+ years
Supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines.
Locations (2)
- Buffalo, New York, United States
- Tonawanda, New York, United States
Responsibilities
- Communicate clearly and professionally with study participants regarding study objectives and ongoing instructions.
- Adhere to site standard operating procedures (SOPs).
- Administer questionnaires and monitor participant compliance with study protocols.
- Respond to participant needs promptly and appropriately.
- Collect and document patient medical history and health conditions.
Requirements
- Associate's degree in healthcare or a related field, or equivalent relevant experience