Clinical Research Associate (West Coast)
Is this job for you?
Build my CV Build your CV and see how well you match this role — and every other one.
The role
The Clinical Research Associate ensures high-quality monitoring of assigned protocols and sites in accordance with the study protocol, SOPs, GCP, and regulatory requirements.
Responsibilities include on-site and remote monitoring visits, site initiation, interim visits, and close-out visits with timely monitoring reports.
Create and maintain study-specific monitoring documentation, train site personnel, and ensure proper source documentation and case report completion.
Oversee regulatory documentation accuracy, support regulatory queries, and manage investigational supplies, dispensing, inventory, and reconciliation.
Monitor site enrollment, protocol deviations, SAEs, laboratory abnormalities, and other activities to ensure compliant trial conduct.
Coordinate with internal teams, sponsors, and external partners, participating in meetings and ensuring proactive communication and issue resolution.
Responsibilities include on-site and remote monitoring visits, site initiation, interim visits, and close-out visits with timely monitoring reports.
Create and maintain study-specific monitoring documentation, train site personnel, and ensure proper source documentation and case report completion.
Oversee regulatory documentation accuracy, support regulatory queries, and manage investigational supplies, dispensing, inventory, and reconciliation.
Monitor site enrollment, protocol deviations, SAEs, laboratory abnormalities, and other activities to ensure compliant trial conduct.
Coordinate with internal teams, sponsors, and external partners, participating in meetings and ensuring proactive communication and issue resolution.
See the full job post
Responsibilities, requirements, skills and benefits — create your free account.
Already have an account? Log in
Similar openings
Other roles that could suit you.