Senior Clinical Research Associate
Job Summary
To enable a world-class R&D organization, the full-time remote Senior Clinical Research Associate will manage protocol level execution of study deliverables, including start-up, execution, and close-out of clinical trials.
Key responsibilities
- Ensure successful execution of study protocols, including site monitoring visits, evaluations, and reporting
- Maintain clinical trial management systems and ensure compliance with federal regulations and Good Clinical Practices (GCPs)
- Coach and mentor Clinical Research Associates (CRAs) while preparing for audits and inspections
Required qualifications
- Bachelor's degree or equivalent in a health-related field (e.g., Medical, Scientific, Nursing, Pharmacy) preferred
- Minimum of 5 years of site monitoring experience
- Strong analytical and critical thinking skills
- Excellent interpersonal skills with the ability to communicate effectively
- Demonstrated business ethics and integrity
Complete Job Description
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