Job Summary
The Clinical Research Associate II (CRA II) position is based in Redwood City, California, and requires the individual to work onsite. This role is integral to overseeing clinical study activities, particularly involving glucocorticoid receptor antagonists and advanced clinical trials in patient populations. The CRA II will be a key link in ensuring that studies are conducted effectively and in compliance with regulatory standards.
Responsibilities
- Monitor clinical study activities to ensure adherence to protocols and regulatory requirements.
- Collate and review study data to ensure accuracy and integrity.
- Maintain strong communication with clinical sites and study teams.
- Assist in the preparation of study-related documents and reports.
- Identify and resolve issues that may arise during study implementation.
Qualifications
- A Bachelor’s or Master’s degree in a scientific discipline or health-related field, or a registered nursing degree.
- A minimum of three years of experience as a Clinical Research Associate.
- Strong knowledge of clinical trial regulations and good clinical practices.
- Excellent organizational and communication skills to manage study activities effectively.
- Ability to work collaboratively in a team-oriented environment.
