Job Description: We are seeking a skilled and motivated Contract Clinical Research Associate (CRA) to join our team in Florida. The CRA will be responsible for monitoring and overseeing clinical trials to ensure compliance with regulatory requirements, Good Clinical Practice (GCP) guidelines, and study protocols. Key duties include site selection, initiation, routine monitoring, and close-out visits, as well as managing data collection and ensuring the integrity of clinical trial data.
Key Responsibilities:
- Conduct site monitoring visits, including pre-study, initiation, routine, and close-out visits.
- Ensure adherence to study protocols, GCP, and regulatory requirements.
- Review and verify case report forms and other data to ensure accuracy and completeness.
- Collaborate with investigators and site staff to resolve issues and ensure trial milestones are met.
- Prepare and submit monitoring reports and maintain essential documentation.
Qualifications:
- Bachelor’s degree in life sciences, nursing, or a related field.
- Minimum of 2 years of experience as a Clinical Research Associate.
- Strong knowledge of GCP and FDA regulations.
- Excellent organizational and communication skills.
- Ability to travel within Florida as required.
Contract Duration: 3 months
