Catalyst is a clinical development organization providing highly customizable clinical research solutions to the global biopharmaceutical industry through two established solutions: Catalyst Flex and Catalyst Oncology. Comprised of more than 500 members, our teams work to provide multi-therapeutic global resourcing and functional services through Catalyst Flex, and a full-service oncology CRO offering through Catalyst Oncology. we’ve built our flexible service model from more than a decade of listening to customers, devising customer-centric solutions, and helping them drive breakthrough clinical development studies leveraging our expert teams and innovative technologies.
**We are looking for oncology focused CRA's that would be comfortable with traveling to both East Coast and West Coast sites**
Job Duties:
As a Senior Clinical Research Associate, you will monitor clinical trial programs and manage regional clinical trial sites to support biological and pharmaceutical developmental programs in a manner consistent with relevant regulations including ICH/GCP and PhRMA guidelines along with Catalyst Clinical Research’s applicable SOPs and working practices. You will collaborate with an assigned clinical research team to provide input on site selection, study initiation procedures, conflict resolution, and audit responses. You will effectively communicate all relevant and important findings with appropriate in-house personnel.
Specific responsibilities will include but are not limited to:
Qualifications:
Catalyst Clinical Research, LLC is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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