Clinical Research Coordinator - Cardiology

Columbia University

United States

August 18, 2021

Description

Clinical Research Coordinator - Cardiology

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  • Requisition no: 516191
  • Work type: Full Time
  • Location: Medical Center
  • School/Department: Medicine
  • Grade: Grade 103
  • Categories: Research (Lab and Non-Lab)

  • Job Type: Officer of Administration

  • Bargaining Unit:
  • Regular/Temporary: Regular
  • End Date if Temporary:
  • Hours Per Week: 35
  • Salary Range: Commensurate with experience
  • Position Summary

    We are looking for a Clinical Research Coordinator to orchestrate research activities for the Cardiogenic Shock program. This will include establishing and maintaining a Cardiogenic Shock database. In addition to being a repository for data collected on Cardiogenic Shock patients enrolled in studies at Columbia, this database will also be designed to facilitate seamless integration into multicenter shock registries like the Cardiogenic Shock Working Group.

    Responsibilities

  • Review new protocols, and consent documents for operational feasibility and work in collaboration with the principal investigators on all study related activities.

  • Explain the clinical research protocols to patients and their families in a manner that is friendly and easily understood and be able to answer questions appropriately.

  • Coordinate multiple projects and obtain proper informed consent, collect data and complete case report forms appropriately.

  • Establish internal and external relationships with local physicians and clinical teams, screen for potential subjects, prepare recruitment plans and revise as necessary to meet target enrollment goals.

  • Ensure that pertinent data is recorded according to protocols.

  • Coordinate the clinical research protocol follow-up visits.

  • Interact appropriately with subjects, team members, and core laboratory personnel as needed.

  • Ensure that regulatory binders are complete and up-to date and ensure protocol events (modifications, renewal, unanticipated problems, terminations) are submitted to the IRB with approval documentation in place.

  • Understand the clinical process, practice GCP and FDA/HHS regulations, and fulfill regulatory and reporting requirements for clinical research protocols.

  • Comply with Columbia University and Hospital policies and procedures related to Clinical Research.

  • Perform other responsibilities as needed.
  • Minimum Qualifications

  • Bachelor's degree or equivalent combination of education and experience, plus at least two years' related experience.
  • Preferred Qualifications

  • Advanced degrees are preferred.
  • Experience working with coordinating research and data collection
  • Phlebotomy skills
  • Fluency in Spanish.
  • Other Requirements

  • Strong communication and organizational skills are required.
  • Participation in the medical surveillance program.
  • Must successfully complete systems training requirements.
  • Equal Opportunity Employer / Disability / Veteran

    Columbia University is committed to the hiring of qualified local residents

    Applications open: Jul 13 2021 Eastern Daylight Time Applications close:

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