Job Summary
The position of Clinical Research Associate (CRA I/II) – FSP is located in Nashville, Tennessee, and is offered on an onsite basis. The primary focus of this role is to enhance global health through various stages of clinical trials while also engaging in regulatory activities and consulting.
Responsibilities
- Oversee different phases of clinical studies including initiation, management, and closure.
- Serve as a point of communication with Investigators and site personnel regarding protocol-related issues.
- Ensure compliance with regulatory requirements and protocols throughout the clinical trial process.
- Document and report findings, addressing any discrepancies promptly.
Qualifications
- Strong understanding of clinical research processes and regulations.
- Proficient communication skills, both verbal and written.
- Ability to work collaboratively with Investigators and site staff.
- Prior experience in clinical research is often preferred.
Parexel provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
