Clinical Research Associate II
Core
Frontline communication with project stakeholders to ensure timelines, targets, and standards of clinical research projects across various therapeutic indications.
Role type
Clinical Research Associate II (On-site Monitoring)
Builds
Clinical trial monitoring and data compliance for pharmaceutical research
Domain
Life Sciences / Clinical Research / Oncology
Deliverable
client delivery
Required skills
On-site monitoring, quality control compliance, investigator relations, investigational product handling, training delivery, site identification, regulatory document support, audit resolution, automated tracking systems
Preferred skills
Oncology study experience, MS Office proficiency
Technologies
Automated tracking systems, MS Office
Responsibilities
Conduct monitoring visits, support quality control and compliance reviews, contact investigators and vendors, handle investigational products, deliver training to site staff, support site identification and feasibility, assist Regulatory Affairs with procurement, prepare for and attend audits
Seniority
Mid-level, independent execution