Job Summary
The Clinical Research Associate plays a crucial role in managing medical recruitment and screening procedures, ensuring adherence to all relevant federal, state, and university regulations. This position is pivotal in the collection and analysis of data from clinical trials, as well as the maintenance of essential regulatory documentation and the provision of educational support to clients and their families.
Responsibilities
- Oversee the recruitment and screening processes for clinical trials.
- Ensure compliance with applicable federal, state, and university regulations.
- Collect and analyze data related to clinical research studies.
- Maintain and organize regulatory documents necessary for trials.
- Educate clients and their families about clinical trial procedures and implications.
Qualifications
- Bachelor’s degree in a relevant discipline with one year of professional experience, or a Master’s degree in an applicable field.
- Strong understanding of clinical research protocols and standards for regulatory compliance.
