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Pennsylvania State University

Land-grant university in University Park, PA

Clinical Trial Research Monitor - Beat Childhood Cancer Research Consortium

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeHershey, PA, USA$59.6k - $95k

About the Job

Requirements

  • A Bachelor's degree and at least one year of relevant experience, or an equivalent combination of education and experience, are required for the general position; additional education and/or experience is required for higher-level placement.
  • For Research Project Manager - Professional placement, a Bachelor's degree is required; no prior relevant work experience is required, though previous relevant work experience may be accepted in lieu of education.
  • For Research Project Manager - Intermediate Professional placement, a Master's degree and at least one year of relevant experience, or an equivalent combination of education and experience, are required.
  • A valid U.S. driver's license and successful completion of a motor vehicle records check are required.
  • Successful completion of standard background checks is required.
  • Candidates must be authorized to work in the United States; Penn State does not sponsor or take over sponsorship of a staff employment visa.
  • A strong background in Clinical Trial Management, Human Subjects Research, and IND/IDE regulatory requirements is expected.
  • Experience working with a team, multiple Principal Investigators, and Phase I/II clinical trial projects is expected.
  • Strong verbal and written communication skills and the ability to multitask and foster collaboration and teamwork are required.

Responsibilities

  • Protect trial participants' rights and wellbeing and ensure reported trial data are accurate, complete, and verifiable against source documents.
  • Serve as the primary contact between investigational sites and BCC leadership.
  • Ensure clinical trials comply with ICH GCP guidelines, local and global regulatory requirements, and BCC standard operating procedures.
  • Build relationships with Principal Investigators, study coordinators, pharmacists, and other site trial personnel to support efficient and smooth clinical-trial management.
  • Foster internal and external relationships to support efficient, timely, and productive project delivery according to study requirements and timelines.
  • Work with Regulatory teammates to understand applicable local and international regulatory requirements for specific clinical trials.
  • Monitor investigational sites according to ICH GCP §5.18 and each BCC study monitoring plan, conducting site initiation, site monitoring, and site close-out visits onsite or remotely as needed.
  • Protect participant rights and wellbeing by checking consent forms, confirming patient eligibility and protocol compliance, checking investigational drug compliance, and reviewing adverse events and serious adverse events; promptly report safety issues to BCC.
  • Verify trial data for accuracy and completeness, and ensure case report form data and queries are completed and resolved according to study timelines in the study monitoring plan.
  • Ensure study drugs are stored, dispensed, accounted for, and reconciled according to the study monitoring plan and protocol.
  • Guide sites in establishing or improving data-collection and data-management processes.
  • Educate enrolling site staff about protocols, electronic data capture, regulatory requirements, and expectations.
  • Travel to BCC hospital sites for monitoring visits approximately every four to six weeks.
  • Operate a motor vehicle as part of job duties.

About the Company

Pennsylvania State University

Land-grant university in University Park, PA

Pennsylvania State University is a multi-campus, land-grant public research university whose mission spans undergraduate and graduate education, research, and public service.

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