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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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to join our Clinical Trials Office team. As a Principal Clinical Research Coordinator (PCRC) you will be responsible for serving as a lead within you respective disease team mentoring new staff, providing
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to join our Clinical Trials Office team. As a Principal Clinical Research Coordinator (PCRC) you will be responsible for serving as a lead within you respective disease team mentoring new staff, providing
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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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advancements tailored to hematological malignancy patients. As a successful candidate you will: · Perform genotyping · Amplify plasmid · Procure reagents/supplies · Master mouse techniques such as