Senior Clinical Research Associate
Core
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards.
Role type
Senior Clinical Research Associate (IC)
Builds
Clinical trial execution and data integrity
Domain
Healthcare / Clinical Research
Deliverable
physical/clinical work
Required skills
Clinical trial monitoring, site management, regulatory compliance, data integrity, GCP standards, clinical trial software proficiency
Preferred skills
Cross-functional collaboration, training and guidance, stakeholder relationship management, problem-solving
Responsibilities
Monitor clinical trial sites for protocol and regulatory adherence, conduct site visits to assess performance and resolve issues, collaborate on data collection and reporting, provide training to site staff and CRAs, build relationships with site personnel and stakeholders
Seniority
Senior, hands-on IC
