Job Summary
The Clinical Research Associate II (CRA II) plays a crucial role in managing various aspects of clinical study sites, ensuring they adhere to guidelines for patient safety and data integrity. This includes responsibilities such as site initiation, monitoring on-site activities, and providing ongoing management of study sites.
Responsibilities
- Conduct independent site visits to monitor progress and compliance.
- Oversee the management of regulatory documentation for studies.
- Facilitate effective communication between site staff and project teams.
- Ensure adherence to clinical research protocols and regulations.
Qualifications
- A bachelor’s degree in a scientific or healthcare-related field is required.
- A minimum of two years’ experience as a Clinical Research Associate in a Contract Research Organization or a similar environment.
- Demonstrated understanding of clinical research regulations and guidelines.
- Strong organizational capabilities to manage multiple tasks efficiently.
- Willingness to travel up to 60% of the time for site visits and meetings.
Precision Medicine 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.
