Job Summary
The Contract Clinical Research Associate (CRA) plays a crucial role in the field of clinical trials and medical research. This position involves overseeing the execution of clinical studies, ensuring compliance with regulatory requirements, and maintaining high standards of quality throughout the research process. The CRA acts as a liaison between the clinical site and the sponsor, ensuring that study protocols are adhered to and that data integrity is preserved.
Responsibilities
- Monitor clinical trial sites to ensure they are following study protocol and regulatory guidelines.
- Conduct site visits to assess the progress of trials and address any issues that may arise.
- Review and verify source documents and case report forms for accuracy and completeness.
- Provide training and support to site personnel regarding study protocols and procedures.
- Maintain accurate records and documentation related to trial activities and site performance.
Qualifications
- Strong background in clinical research and knowledge of Good Clinical Practice (GCP) guidelines.
- Relevant experience as a Clinical Research Associate or in a similar role.
- Excellent communication and interpersonal skills to effectively collaborate with diverse teams.
- Attention to detail and the ability to manage multiple tasks efficiently.
- Bachelor’s degree in a life sciences field or a related discipline is preferred.
Brio Group 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.
