Job Summary
The Clinical Research Associate/Coordinator I plays a crucial role in supporting clinical trials by assisting with the planning, implementation, and monitoring of clinical research studies. This entry-level position focuses on ensuring compliance with regulatory requirements and study protocols while facilitating effective communication among study participants and stakeholders.
Responsibilities
- Assist in the preparation and execution of clinical study protocols and related documentation.
- Monitor study progress and ensure adherence to regulatory standards and protocol compliance.
- Communicate with investigators, study participants, and regulatory bodies to facilitate study operations.
- Collect, manage, and analyze data related to clinical trials.
- Prepare reports and documentation for regulatory submission and approval.
- Participate in site visits and audits to ensure compliance with study requirements.
Qualifications
- A Bachelor’s degree in a relevant scientific or healthcare field.
- Basic knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
- Strong organizational skills and attention to detail.
- Good communication skills, both verbal and written.
- Ability to work collaboratively with diverse teams and stakeholders.
- Familiarity with clinical trial processes is preferred but not required.
Buck Institute 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.
