Senior Clinical Research Associate
Core
Monitor clinical studies at investigative sites or remotely to ensure trials are conducted, recorded, and reported in accordance with protocols, SOPs, and regulatory requirements.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data and compliance reports for pharmaceutical, biotechnology, and medical device organizations
Domain
Healthcare / Clinical Research / Oncology
Deliverable
client delivery
Required skills
Clinical monitoring, ICH-GCP knowledge, regulatory compliance, study coordination, nursing background
Preferred skills
Oncology monitoring experience
Technologies
None stated
Responsibilities
Monitor progress of clinical studies at investigative sites or remotely; Ensure clinical trials are conducted, recorded, and reported in accordance with protocol, SOPs, and regulatory requirements
Seniority
Senior, hands-on IC
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