Job Summary
The Clinical Research Associate II (CRA II) plays a vital role in overseeing designated investigational sites throughout the entire clinical trial process. This position requires effective management of site activities to ensure compliance with regulatory standards and quality assurance throughout the trials.
Responsibilities
- Monitor the performance of assigned investigational sites during clinical studies.
- Ensure adherence to protocols and compliance with regulatory requirements.
- Collaborate with site staff to support the execution of clinical trials.
- Facilitate communication between study sites and the sponsor.
- Document findings and report on site performance and issues.
Qualifications
- A degree in a relevant life science discipline.
- Prior experience as a Clinical Research Associate.
- Knowledge of Good Clinical Practices (GCP) and regulatory guidelines.
- Strong organizational and communication skills.
- Ability to work independently and as part of a team.
Caidya 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.
