Clinical Research Associate II
Core
Conduct onsite monitoring visits, manage study startup, and verify source documents for clinical studies in oncology, hemophilia, infectious diseases, and GI.
Role type
Clinical Research Associate II (Phase II/III)
Builds
Clinical studies for pharmaceutical/biotech clients
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Onsite monitoring, CRF review, source document verification, query resolution, site communication, feasibility research, regulatory document preparation
Preferred skills
Phase II/III experience, oncology/hemophilia/infectious diseases/GI therapeutic area knowledge, MS Office proficiency, travel ability
Technologies
MS Office
Responsibilities
Conduct and report onsite monitoring visits, perform study startup activities, review CRFs and verify source documents, resolve queries, manage site communication, support regulatory submissions
Seniority
Mid-level, hands-on IC