Pranav Hegde

Experience

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  Stanford University

  Jun 2019 - Feb 2022

  ● Recruited and/or managed over 15 clinical trials, including for the now approved 18F-DCFPyL and Ga-PSMA-11 tracers for the detection and diagnosis for prostate cancer ● To date, recruited over 250 patients to participate in appropriate phase II/Phase III Clinical Trials ● Meet routinely with the principal investigator of the study to ensure proper patient, protocol, and safety adherence outlined for proper study conduct ● Serve as the main contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out ● Determine the eligibility of study participants by gathering source documentation from medical databases or outside healthcare facilities ● Gather consent from study participants according to protocol and answering any questions regarding the clinical trial to ensure full transparency ● Ensure that participants adhere within research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure Institutional Review Board renewals are completed. ● Coordinate collection of study data from PACS and EPIC and relay them to the appropriate referring physicians and oncologists ● Collect and manage patient and laboratory data for clinical research projects. Manage Research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms. ● Manage reimbursements and additional costs included in the clinical trial. ● Recording essential documentation of patient and research data per institutional and regulatory requirements. ● Documenting and addressing any adverse events or protocol deviations to maintain study integrity Show less

  • Clinical Research Coordinator II

    Jun 2021 - Feb 2022

  • Clinical Research Coordinator Associate

    Jun 2019 - May 2021
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  Genentech

  Feb 2022 - Feb 2023

  US Clinical Operations Lead

  Assist in operational activities from study start-up through database lock: including feasibility, regulatory document management, systems maintenance, site support, and vendor management.Improve study engagement at the site level which includes, but is not limited to: promoting recruitment endeavors, niche advertising, and improving site-industry communication.Use different databases such as eTMF, CTMS, and RAVE EDC to ensure proper documentation from the site to patient level.

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  Foothill College

  Jan 2023 - Feb 2024

  Student
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  Mass General Hospital

  Feb 2024 - now

  Graduate Student