Description
This role involves assisting in the conduct of clinical trial activities in accordance with applicable regulations.
Key responsibilities include:
- Building relationships with study team members, investigators, and office staff
- Screening, recruiting, and enrolling research subjects
- Scheduling patient visits and procedures
- Collecting patient history and performing data entry
- Coordinating follow-up care and laboratory procedures
- Adhering to IRB-approved protocols and company policies
The role requires strong interpersonal and team-building skills, logical thinking, and adaptability.
The potential base pay range for this role is $35,800.00 - $89,400.00 per year.