Job Summary
The Clinical Research Associate II position is open across all locations in the United States, specifically based in Richmond, Virginia. This onsite role is dedicated to enhancing global health through comprehensive involvement in clinical trials, regulatory processes, and consulting. The CRA plays a vital role in overseeing the management and closure of clinical trial sites, ensuring that the safety of patients is prioritized throughout the study.
Responsibilities
- Oversee the conduct of clinical trials at assigned investigator sites.
- Ensure compliance with regulatory requirements and study protocols.
- Conduct site monitoring visits to assess progress and participant safety.
- Coordinate the close-out of clinical trial sites efficiently.
- Collaborate with investigators and site staff to facilitate a smooth trial process.
Qualifications
- A background in clinical research or a related field.
- Experience with trial monitoring and regulatory compliance.
- Strong communication and organizational skills.
- Ability to work independently and in a team environment.
- Knowledge of GCP and ICH guidelines.
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.
