Job Summary
The Senior Clinical Research Associate (CRA) position focuses on enhancing global health through the management and oversight of clinical trials and regulatory processes. This role involves working collaboratively as part of site teams, which include Principal Investigators, Study Coordinators, and Pharmacists, among others.
Responsibilities
- Ensure the compliance and integrity of clinical trials by conducting site visits and monitoring study progress.
- Collaborate effectively with site personnel to facilitate the smooth execution of studies.
- Assist in the preparation and submission of regulatory documentation.
- Provide training and support to site staff to maintain adherence to protocols.
- Evaluate data collected during trials, ensuring accuracy and prompt reporting of findings.
Qualifications
- A Bachelor’s or Master’s degree in a relevant field, such as life sciences or nursing.
- Experience in clinical research or related areas, demonstrating an understanding of the clinical trial process.
- Strong communication and interpersonal skills to work with diverse teams.
- Detail-oriented with excellent organizational abilities.
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.
