Clinical Research Associate II
Core
On-site monitoring of clinical studies across various therapeutic indications, ensuring data integrity, compliance, and site performance.
Role type
Clinical Research Associate II (IC)
Builds
Clinical trial data and regulatory compliance for sponsors
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Source data verification, adverse event reporting, protocol deviation management, site selection and initiation, close-out visits, investigator training, regulatory submission support, supply chain management, audit preparation and resolution
Preferred skills
Oncology, GI, radio-pharm experience
Technologies
MS Office
Responsibilities
Conduct routine monitoring visits (site selection, initiation, close-out), verify source data, manage adverse events and protocol deviations, reconcile Investigator Site Files, prepare for and participate in audits, train site investigators, manage clinical study supplies
Seniority
Mid-level, hands-on IC