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11 May 2021

Full-Time Clinical Research Coordinator I

oconnors1 – Posted by oconnors1 Philadelphia, Pennsylvania, United States

Job Description

Job Summary

The successful candidate will join the research teams of Dr. Laura Vella and Dr. Brian Fisher in the Pediatric IDEAS Research Group  at Children’s Hospital of Philadelphia. Dr. Vella’s research is translational and focuses on vaccine responses in settings of immune health and immune compromise. Dr. Fisher’s research focuses on infections in children with immunocompromising conditions.

The applicant is expected to work comfortably as part of a research team. The successful applicant should have strong writing, organizational, and analytical skills. A collaborative working style is required. The successful applicant will be responsible for leading specific projects. The candidate will be a member of the Pediatric IDEAS Research Group, a collaborative group of investigators within the Center for Pediatric Clinical Effectiveness (CPCE) at CHOP. The mission of the Pediatric IDEAS Research Group is to perform rigorous clinical and translational research that generates evidence on the prevention and treatment.


Job Responsibilities

Core responsibilities

  • Adhere to an IRB approved protocol
  • Participate in the informed consent process of study subjects
  • Support the safety of clinical research patients/research participants
  • Coordinate protocol related research procedures, study visits, and follow-up care
  • Screen, recruit and enroll patients/research participants
  • Maintain study source documents
  • Report adverse events
  • Understand good clinical practice (GCP) and regulatory compliance
  • Educate subjects and family on protocol, study intervention, etc.
  • Comply with Institutional policies, standard operating procedures (SOPs) and guidelines
  • Must comply with federal, state, and sponsor policies

Related responsibilities

  • Manage essential regulatory documents
  • Register study on
  • Complete case report forms (paper & electronic data capture) and address queries
  • Submit documents to regulatory authorities (e.g. IRB, FDA, etc.) and/or review/monitoring boards (ie, DSMB, independent safety officer)
  • Facilitate pre-study, site qualification, study initiation, and monitoring visit
  • Facilitate study close out activities
  • Coordinate research/project team meetings
  • Collect, process and ship laboratory specimens
  • Schedule subject visits and procedures
  • Retain records/archive documents after study close out

How to Apply

Interested applicants should apply on the CHOP Careers site:

Job Categories: Equal Opportunities. Job Types: Full-Time. Salaries: Not Disclosed.

Job expires in 51 days.

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