Clinical Research Associate 3
Core
Senior Clinical Research Associate leading clinical trial monitoring tasks to ensure adherence to protocols, regulatory requirements, and GCP standards.
Role type
Senior IC Clinical Research Associate
Builds
Clinical trial execution and data integrity for pharmaceutical sponsors
Domain
Clinical Research / Life Sciences
Deliverable
physical/clinical work
Required skills
Clinical trial monitoring, site management, data integrity, regulatory compliance, GCP standards, clinical trial software proficiency
Preferred skills
Cross-functional collaboration, training and guidance, stakeholder relationship building
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