Job Summary
The Clinical Research Associate (CRA) plays a crucial role in supervising and managing assigned investigative sites, ensuring compliance with relevant regulations and guidelines in the realm of therapeutics development.
Responsibilities
- Oversee and monitor the activities of specific investigative sites.
- Ensure adherence to all applicable regulations and standards during the research process.
- Act as the primary point of contact for site staff and facilitate communication between the site and the sponsor.
- Review and verify study documentation for accuracy and completeness.
- Assist in the training of site personnel and provide ongoing support as needed.
Qualifications
- Bachelor’s degree in a scientific field, pharmacy, nursing (RN), or a Bachelor of Science in Nursing (BSN) or equivalent experience.
- Strong understanding of clinical research processes and regulatory requirements.
- Excellent communication skills, both verbal and written.
- Ability to work effectively in a team environment.
- Proficiency in data management and reporting.
