CRA 2/Senior CRA 1
Core
Lead and execute site monitoring visits (selection, initiation, routine, close-out) to ensure clinical trials are executed with excellence, compliance, and a strong focus on patient outcomes.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trials for life sciences and healthcare industries
Domain
Clinical Research / Life Sciences
Required skills
GCP/ICH guidelines knowledge, site monitoring, patient recruitment, data integrity management, risk identification, regulatory approval tracking, study documentation
Preferred skills
CNS, Cardiovascular, Obesity, MASH/NASH therapeutic area experience
Technologies
CTMS systems, 1572 process
Responsibilities
Lead and execute site monitoring visits; Build strong relationships with investigative sites; Ensure protocol compliance and data integrity; Proactively identify risks and resolve issues; Track and manage study progress; Maintain accurate study documentation; Collaborate with cross-functional teams
Seniority
Senior, hands-on IC