An employer is looking for two Clinical Research Coordinators sitting the Westwood Los Angeles area. These roles will be supporting thecompany's hematology malignancy clinical trials. This position is necessary to ensure the proper and timely reporting of research data collected on various research studies. This includes reporting of research data to sponsor and to the IRB. With advances in the research study start-up process and increased availability of research trials, the disease team is opening new studies and enrolling multiple patients at an impressive rate. Moreover, with the initiation of remote monitoring activities due to COVID-19, the role of the CRC now includes preparation and participation in remote monitoring visits. This has some active involvement than our previous on-site monitoring requirements as all source documents must be available remotely for sponsor partners. This position ensures the collection and submission of data to sponsoring agency meets protocol requirements. This role assists in quality control and quality assurance activities to maintain 'audit-ready' status.
- Oncology clinical research background
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.