Job Summary
Premier Research is seeking a dedicated Clinical Research Associate (CRA) to join our Clinical Monitoring and Site Management team in California, Missouri. This role primarily involves executing various clinical research activities and ensuring compliance with regulatory standards and protocols.
Responsibilities
- Oversee and conduct clinical trial activities while monitoring site performance and patient safety.
- Attend and actively participate in Investigators’ Meetings.
- Provide essential support in site management and facilitate communication with site staff.
- Ensure all necessary documentation is properly managed and maintained throughout the study.
- Conduct regular site visits to monitor trial progression.
Qualifications
- A degree in a related field, such as Nursing or a similar healthcare discipline.
- Relevant work experience in clinical research or equivalent qualifications is required.
- Strong understanding of regulatory requirements and GCP guidelines.
- Excellent communication and organizational skills.
- Ability to work collaboratively within a team-oriented environment.
