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Public Administration Analyst - Clinical Research
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- The Clinical Research Specialist (CRS) will work with the Network Clinical Research Team and UCLA study teams that support the JCCC Clinical Research Unit, the Translational Research in Oncology-US Network (TRIO-US), in the set-up and conduct of
- The CRS will ensure that all study safety data (i.e. MedWatch's, SAEs, protocol waivers/exceptions, deviations/violations) are processed, recorded and reported properly to the Sponsor and IRB and/or FDA, as appropriate.
- Assist with the coordination of study start-up for Network clinical trials; work with the UCLA Study Teams, IRB and Pharmaceutical sponsors and CROs for network site participation.
- In conjunction with the Team Lead and/or Regulatory Manager, establish and schedule study start-up dates and processes for the Network
- Assist Study Sponsors and Sponsor representatives with the distribution of required study supplies to the appropriate Network sites for study start-up and ongoing study needs.
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