U

University of Pennsylvania

Ivy League university in Philadelphia, PA

Clinical Research Coordinator C

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timePhiladelphia, PA, USA$63.1k /yrIn-person

About the Job

Requirements

  • A Bachelor of Science degree and 4 to 6 years of experience, or an equivalent combination of education and experience, is required.
  • Practical experience coordinating the day-to-day activities of multiple therapeutic research protocols is required.
  • Effective verbal and written communication skills are required.
  • The ability to learn new methods quickly and multitask is required.
  • The ability to work as part of a team and independently is required.
  • The ability to work flexible hours is required.
  • Working knowledge of Title 21 Code of Federal Regulations, International Conference of Harmonisation, and Good Clinical Practice guidelines is required.

Responsibilities

  • Coordinate the conduct of Phase I–IV clinical trials.
  • Participate in audits conducted by study sponsors, Clinical Research Organizations, the FDA, and other entities as required.
  • Participate in developing investigator-initiated protocol case report forms and progress notes.
  • Conduct initiation, monitoring, and closeout visits with sponsors and/or Clinical Research Organizations.
  • Organize and maintain sponsor- or Clinical Research Organization-required documentation, including source documentation, case report forms, study and regulatory binders, and patient binders.
  • Resolve data queries with sponsors and Clinical Research Organizations.
  • Recruit, screen, and enroll potential study patients as specified by protocol.
  • Process and ship blood, urine, and serum specimens for each trial.
  • Schedule patient visits and any necessary testing.
  • Attend Investigator Initiation meetings.
  • Obtain pathology slides and ship them to the sponsor or independent reviewer according to protocol guidelines.
  • Obtain records required to complete case report forms.
  • Maintain vigilance in patient safety, protocol compliance, and data quality.
  • Adhere to University of Pennsylvania, ICF, and FDA guidelines.
  • Use the electronic medical record for research tracking and optimization.
  • Start up and support multisite trials.
  • Operationalize clinical research protocols and build partnerships to execute them.
  • Participate in case report form testing and possibly design.
  • Prepare and process all Institutional Review Board documentation, including submissions, continuing reviews, amendments, and adverse event reporting.
  • Prepare and process regulatory documentation with pharmaceutical companies and Clinical Research Organizations.
  • Organize and maintain regulatory documents required by sponsors or Clinical Research Organizations, including institutional forms, FDA Form 1572, deviation memos, physicians’ and coordinators’ curricula vitae and medical licenses, and records of Institutional Review Board certification and compliance.
  • Resolve regulatory queries with the Institutional Review Board, study sponsors, and Clinical Research Organizations.

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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