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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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) 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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supervision of the Principal Investigator, or designee, the RA II directs the animal work of a laboratory and/or undertakes animal (mouse) research projects in collaboration with academic supervisor, making
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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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through cutting-edge research. Under the direct supervision of the Principal Investigator or designee, the Research Associate I will play an integral role in advancing innovative research within the Thymus
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highly active here. The primary goal of this position is to implement novel MRI and image processing techniques for the application in radiation therapy, including imaging guidance of radiotherapy
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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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through cutting-edge research. Under the direct supervision of the Principal Investigator, or designee, the Research Associate I will perform a variety of research experiments. The van den Brink Laboratory
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. The team behaves as EDC experts and maintains primary responsibility over form design, development, validation, and updates on a recurring basis until study closure. Key Responsibilities include: Work
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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