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3 Days AgoSaved
Remote
7 Locations
108K-140K Annually
Senior level
108K-140K Annually
Senior level
Biotech
Lead site monitoring and management for clinical studies, ensuring regulatory compliance, data integrity, SAE tracking, and audit readiness. Conduct initiation, routine, and closeout visits; prepare trip reports; manage small projects, train/mentor junior staff, liaise with vendors, assist protocol/CRF development, and perform local project coordination as assigned. Frequent travel (~50%+), Spanish language ability required.
Reposted 4 Days AgoSaved
In-Office or Remote
15 Locations
105K-117K Annually
Mid level
105K-117K Annually
Mid level
Biotech
Lead and support clinical trials as a CRA II, ensuring compliance, monitoring sites, and managing data integrity with a focus on ophthalmology studies.
Top Skills: Electronic Data Management Systems
Reposted 12 Days AgoSaved
In-Office or Remote
15 Locations
105K-117K Annually
Mid level
105K-117K Annually
Mid level
Biotech
As an Oncology CRA II, you'll monitor clinical trials, ensure protocol adherence, manage data integrity, and support site management tasks, while collaborating with teams and vendors.
Top Skills: Data Management SystemsElectronic Data Collection
Reposted 18 Days AgoSaved
In-Office or Remote
10 Locations
108K-140K Annually
Senior level
108K-140K Annually
Senior level
Biotech
The Senior CRA 2 is responsible for site monitoring, site management, ensuring compliance with regulatory requirements, managing study activities, and leading clinical trials for the company.
Top Skills: Case Report Forms (Crfs)Clinical MonitoringClinical Trial ReportsData Review GuidelinesRegulatory Guidelines
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