Jobs · Analyst · Pennsylvania

Clinical Research Coordinator A/B (Pregnancy & Perinatal Research Center)

University of Pennsylvania · Philadelphia, PA · 1 mo ago
Analyst$47k–$53k/yrFull-time

About the role

The Clinical Research Coordinator will be responsible for all aspects of study coordination including subject recruitment, detailed data entry, collecting biospecimens, subject visits and follow-up, and regulatory documentation.

Responsibilities

  • Clinical Research Coordinator A:
    • Detailed screening of patients for eligibility across multiple studies
    • Consenting of patients into multiple studies
    • Collaborate with clinical team as necessary to provide a positive encounter
    • Provide clinical services, including phlebotomy and obtain biospecimens as required by the protocol
    • Intercept and respond to study participants phone calls
    • Perform telephone follow-up per study protocol
    • Data collection and management in accordance with study protocol and the maintenance of source documents and case report forms
    • Maintain study compliance and integrity through close collaboration with nurse coordinator and investigators as well as the patient
    • Respond to database queries and chart reviews as necessary
    • Congnorate with community partners as needed to encourage recruitment and retention
  • Clinical Research Coordinator B:
    • Coordinate scheduling of study participant visits with study investigators and nurse practitioners as per protocol
    • Ensuring all tests and assessments at each visit are performed, reporting adverse events and ensuring review and appropriate follow-up by investigator
    • Prepare detailed documentation of study activities

*Position contingent upon continued funding*

Qualifications

  • Clinical Research Coordinator A: BS degree and 1-2 years related experience in research and clinical study methodologies or equivalent combination of education and experience required. Must be able to work flexible hours.
  • Clinical Research Coordinator B: BS degree and 2-3 years related experience in research and clinical study methodologies or equivalent combination of education and experience required. Must be able to work flexible hours.

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