CRA 2, Internal Medicine, Biotech
Is this job for you?
Build my CV Build your CV and see how well you match this role — and every other one.
Track your applications on mobile The free Whileresume app, on iPhone and Android.
The role
Conduct site visits including site selection, initiation, monitoring, and close-out to ensure trials are executed per protocol.
Ensure ongoing trial conduct aligns with GCP, ICH guidelines, and sponsor requirements.
Coordinate communications with site staff, resolve queries, and manage issue escalation.
Verify source data, maintain essential regulatory documents, and support regulatory submissions as needed.
Collaborate with cross-functional teams to uphold data quality and patient safety.
Identify risks, implement corrective actions, and contribute to trial timelines and milestones.
Ensure ongoing trial conduct aligns with GCP, ICH guidelines, and sponsor requirements.
Coordinate communications with site staff, resolve queries, and manage issue escalation.
Verify source data, maintain essential regulatory documents, and support regulatory submissions as needed.
Collaborate with cross-functional teams to uphold data quality and patient safety.
Identify risks, implement corrective actions, and contribute to trial timelines and milestones.
See the full job post
Responsibilities, requirements, skills and benefits — create your free account.
or
Already have an account?
Log inYou might also like these jobs
No closely matching jobs yet — here are the most recent ones.