Clinical Research Associate / Senior Clinical Research Associate
Core
Conduct onsite and remote monitoring visits, perform CRF review and source document verification, and manage clinical sites for Phase II/III AMG studies.
Role type
Senior Clinical Research Associate (IC)
Builds
Clinical trial data integrity and site compliance for pharmaceutical sponsors
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Independent onsite monitoring, CRF review, source document verification, query resolution, site identification, site management, study ownership, training of junior CRAs
Preferred skills
Oncology, Hematology, Infectious/Rare/Gastro-intestinal Diseases experience, Switzerland experience, French/Italian language skills
Technologies
MS Office
Responsibilities
Conduct onsite and remote monitoring visits, Perform CRF review and source document verification, Manage site communication and relationships, Assist in training less experienced CRAs
Seniority
Senior, hands-on IC
