Clinical Research Associate II
Core
Partner with investigators and site staff to ensure appropriate conduct of clinical trials, driving data integrity, compliance, and study performance.
Role type
Senior Clinical Research Associate (monitoring)
Builds
Clinical trial execution and data integrity
Domain
Biopharmaceuticals / Clinical Research
Required skills
Clinical trial monitoring, site evaluation, protocol compliance, risk assessment, patient recruitment strategies, regulatory knowledge (ICH/GCP), data quality assurance, investigator management
Preferred skills
Tertiary qualification in health-related disciplines, therapeutic area knowledge, mentoring experience
Technologies
CRM tools
Responsibilities
Conduct site evaluation, training, routine, and closure monitoring; align and train site staff and principal investigators; ensure audit and regulatory inspection readiness; manage investigator payments; identify and evaluate potential investigators/sites; proactively assess and resolve site risk signals; ensure timely data submission and safety event reporting.
Seniority
Senior, hands-on IC