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/Modality Team Chairs, and Study Investigators. Principal Clinical Research Coordinators/Clinical Trial Portfolio Leads (CTPLs) serve as leads within their disease teams, mentoring staff, providing guidance
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clinical protocol development for the City of Hope Thoracic Oncology Program. Under the direction of the Division Chief, Dr. Christine Lovly, you will work closely with laboratory and clinical researchers
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strategies including mechanisms of resistance. As a successful candidate, you will: Under minimal direction of the Principal Investigator, direct the work of a laboratory including supervision of technical lab
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and Technology Training Spend significant time in the lab conducting meaningful research under the guidance of experienced faculty and Principal Investigators (PIs). 🧬Focused Study in Disease Biology
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will also attend lab manager meetings when notified and communicate key updates to the laboratory and the principal investigator. As a successful candidate, you will: Utilize laboratory equipment and
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genetically engineered models, patient-derived samples, and multi-omic platforms to uncover therapeutic vulnerabilities and molecular biomarkers in leukemia and lymphoma. Serve as principal investigator
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) to all applicable regulatory agencies (FDA, OBA, RAC, NIH, NCI) has been completed in a timely manner. Reviews the original protocol and all amendments, noting dates, changes in eligibility criteria, and
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protocols, ensuring compliance with federal regulations and cancer center grant requirements. They serve as resources for City of Hope researchers and committee members, interacting regularly with Principal
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, Good Clinical Practices (GCP), and regulatory standards. Key Responsibilities Lead the build, implementation, and ongoing optimization of the Clinical Trial Management System (CTMS). Serve as the primary
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through cutting-edge research. City of Hope has a Research Associate I opportunity available. Under the direct supervision of the Principal Investigator, or designee, the Research Associate I performs a