Clinical Research Coordinator - CCTI

Columbia University

United States

July 8, 2021

Description

Clinical Research Coordinator - CCTI

Back Apply Share

  • Requisition no: 515070
  • 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: n/a
  • Regular/Temporary: Regular
  • End Date if Temporary: n/a
  • Hours Per Week: 35
  • Salary Range: Commensurate with experience
  • Position Summary

    The Columbia Center for Translational Immunology (CCTI) at Columbia University Irving Medical Center (CUIMC) is seeking a highly motivated and talented Clinical Research Coordinator to join our team. The main topic of this research is a pilot clinical trial using T‐cell alloreactivity and chimerism to guide immunosuppression minimization in intestinal transplantation. Primary responsibilities include consenting patients and collection of clinical specimens and data before and after organ transplantation.

    Responsibilities

  • Identify, recruit, and consent eligible participants; conduct visits as outlined in study protocols and in accordance with Good Clinical Practices (GCP) and HIPAA guidelines.
  • Perform research‐related services including coordinating and scheduling study visits, and making telephone calls.
  • Responsible for data collection, entry and transmission; specimen collection, processing, storing and shipping.
  • Collect, transport, process and shipping blood, lymphoid tissue, intestinal tissue, bone marrow and stool samples in accordance with federal, state and institutional policies, as well as delineated in sponsor's protocol.
  • Interface with various hospital departments including medical records, radiology, nursing, information technology services, and others as needed.
  • Coordinate the collection of all research data points as assigned through research visits, chart abstraction or telephone.
  • Consult with EPIC medical records and UNOS organ donor database to obtain pertinent information of patient and the donor, including age, sex, HLA typing, immunosuppression regimen, rejection and infection episodes, DSA development, and onset of other clinical complications.
  • Perform venipuncture as needed in the collection of blood samples using standard sterile technique.
  • Ensure the appropriate tests, procedures and laboratory tests are completed. Ensure all relevant clinical staff are informed of research participation.
  • Ensure regulatory documents and administrative files for each protocol are up to date. Create and maintain patient research records and enter research data into a centralized database program and other study specific electronic databases.
  • Attend and participate in Investigator, site initiation and monitoring meetings as assigned.
  • Report to the Principal Investigator and Human Studies Research Manager of the CCTI within the Department of Medicine at Columbia University.
  • Adhere to assigned research protocols and manual of operation set forth by the sponsor, maintain screening and randomization logs and handle correspondence appropriately.
  • Responsible for participating in on‐call activities to cover research activity off‐hours.
  • Perform other related duties as needed.
  • Minimum Qualifications

  • Bachelor's degree or equivalent in education, training and experience, plus two years of related experience
  • Experience in Clinical Research and Patient Care Setting
  • Excellent interpersonal skills, written, verbal, organizational and communication skills
  • Possess and maintain a Phlebotomy certification
  • Self‐directed and able to make independent decision within the parameters of all federal, state, institutional and departmental guidelines

  • Detail oriented and able to multi‐task.

  • Self‐motivated with ability to work independently as well as part of a team

  • Proficiency with Microsoft Word, Excel, PowerPoint and data management files required

  • Preferred Qualifications

  • Bachelor's degree or equivalent in healthcare, life sciences, medical technology, or related fields

  • Qualified to take examination for ACRP or SOCRA certification

  • Other Requirements

  • Contact with patients and/or human research subjects
  • Potential bloodborne pathogen exposure
  • Participation in the medical surveillance program
  • Successful completion of applicable compliance and systems training requirements
  • Equal Opportunity Employer / Disability / Veteran

    Columbia University is committed to the hiring of qualified local residents.

    Applications open: Jun 07 2021 Eastern Daylight Time Applications close:

    Back Apply Share

    Share this via:
  • Facebook
  • Twitter
  • LinkedIn
  • Email
  • AddThisMore

    Similar Jobs

    Columbia University

    United States May 12, 2021

    Add to favorites Read more...

    Clinical Research Coord I

    Clinical Research Coord I The primary role of this position is to support clinical research involving women, their families and clinical staff as it relates to clinical research Complete certification requirements for assigned protocols Complete...

    New York University School of Medicine

    United States 4 days ago

    Add to favorites Read more...

    Research Associate

    Facilitate collection of biofluid research specimens for clinical trials by providing clinical collection materials to study team personnel as requested. Maintain basic knowledge of research study design and clinical research specimen collection procedures associated with...