About this role
Field Senior Clinical Research Associate at Namsa. Location: United States. Role: monitoring sites, managing documents, conducting visits Requirements: Ensure human subject protection and GCP compliance, coordinate and conduct site monitoring and start-up activities, manage study documents and metrics; preferred 5+ years clinical trial experience and 3+ years monitoring experience. Category: Research and Development (R&D) Seniority: Senior Level Tools: Clinicaltrials.gov Certifications: socra, acrp Commitment: Full Time Workplace: Field Languages: English