Experienced Clinical Research Associate (Senior / CRA II)
Core
On-site monitoring of clinical studies across various therapeutic indications, ensuring data integrity, compliance, and site performance.
Role type
Senior Clinical Research Associate (CRA II)
Builds
Clinical trial data integrity and regulatory compliance for sponsors
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Source data verification, site selection and initiation, adverse event reporting, protocol deviation management, investigational product accountability, TMF/ISF reconciliation, site audit preparation, site training
Preferred skills
Oncology indication experience
Technologies
MS Office
Responsibilities
Conduct routine monitoring visits (site selection, initiation, close-out), verify source data, manage adverse events and protocol deviations, reconcile study documents and supplies, prepare for and participate in site audits, train site investigators
Seniority
Mid-level, hands-on IC
