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.
