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Principal Clinical Research Coordinator - Orange County Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes
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drug response. As a successful candidate, you will: Consult with Principal Investigator, Staff Scientist, academic researchers, pharmaceutical/biotech company researchers, and/or postdoctoral scholars
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, shaping the future of medicine through cutting-edge research. Under the direct supervision of the Principal Investigator, or designee, the Research Associate I performs a variety of routine and increasingly
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with Quality Control (QC) and Quality Assurance (QA) groups to ensure cGMP compliance. Qualifications: · Bachelors degree with 2-3 years of post-degree laboratory experience or a Masters degree
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general supervision of the Principal Investigator, or designee, the RA II directs the work of a laboratory or undertakes research projects in collaboration with academic supervisor, making innovative
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, Ph.D. Under general supervision of the Principal Investigator, or designee, the Research Associate II (RAII) directs the work of a laboratory or undertakes research projects in collaboration with
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. · Master's or PhD degree in biology or chemistry preferred. · Experience in biotechnology or pharmaceutical industry. · Proficiency in cell viability, Flow Cytometry Assays, ELISA, RT-PCR, and
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ordering, inventory, and other essential lab functions. Keep detailed and accurate logs of experimental design and primary data, analysis, and synthesis. Prepare data presentations and manuscripts
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/research staff, Principal Investigators. Ensure quality assurance: of banked specimens. Adhere to regulations: regarding protected health information (PHI), IRB, and HIPAA. Maintain compliance: with City of
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. · Act independently to determine methods and procedures of new projects. Qualifications: · Bachelors degree in a scientific discipline or equivalent with a Masters degree preferred. · 2-5