U

University of Pennsylvania

Ivy League university in Philadelphia, PA

Clinical Research Coordinator B

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timePhiladelphia, PA, USA$53.4k /yrIn-person

About the Job

Requirements

  • A Bachelor of Science and 2 to 3 years of experience, or an equivalent combination of education and experience, are required.

Responsibilities

  • Coordinate clinical research studies in the Division of Nuclear Medicine in the Department of Radiology and support research activities, including ongoing investigator-initiated and industry-sponsored trials and studies in development or start-up.
  • Take over coordination of ongoing trials involving investigational radiopharmaceuticals for therapeutic use or PET imaging studies in cancer, addiction, infection, cardiology, and neurology.
  • Work with Radiology investigators and investigators from referring departments, including Oncology, Cardiology, Neurology, and Psychiatry, to conduct clinical trials.
  • Initiate and conduct participant screening, recruitment, enrollment, coordination, and scheduling of research procedures and visits; coordinate with referring clinics on joint projects, screening, imaging visits, and complex imaging visits involving multiple investigational radiopharmaceuticals and specialized blood and image analysis.
  • Process, test, and handle blood, urine, and tissue samples for in-house research projects and multicenter clinical trials.
  • For therapeutic-intervention trials, manage recruitment, therapy coordination, follow-up visits, and data and regulatory management of study records.
  • Organize, maintain, and update research documentation, including source documentation, case report forms, research charts, and regulatory files.
  • Collect, review, and report study data by completing electronic or paper case report forms, entering data electronically, and resolving data queries.
  • Abstract medical record information from subjects’ electronic medical records, interviews, and questionnaires for entry into research databases, including REDCap, CTMS, and electronic data-capture programs specified by study sponsors.
  • Enter orders and schedule study-related visits in PennChart, other Penn radiology systems, and sponsor-provided electronic platforms.
  • Prepare and process regulatory documents for regulatory committees from study start-up through completion.
  • Interact with study sponsors and prepare for and participate in study audits, clinical trial initiation visits, monitoring visits, and closeout visits.
  • Perform other duties and responsibilities as assigned.

About the Company

University of Pennsylvania

Ivy League university in Philadelphia, PA

The University of Pennsylvania is a private Ivy League research university in Philadelphia. It comprises twelve undergraduate, graduate, and professional schools, including the Wharton School, Perelman School of Medicine, and Penn Carey Law.

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