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.
