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Clinical Research Coordinator I

Company: Columbia University
Location: New York
Posted on: June 12, 2021

Job Description:

  • Requisition no: 514617
  • Work type: Full Time
  • Location: Medical Center
  • School/Department: Obstetrics and Gynecology
  • Grade: Grade 104
  • Categories: Administrative Support, 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:

Position Summary

The primary role of this position is to support clinical research involving Maternal Fetal Medicine Research. The employee will interact with pregnant women, their families and clinical staff as it relates to clinical research protocols and clinical trials, industry funded and grant funded, being implemented in the inpatient and outpatient setting. The inpatient setting includes labor and delivery, ante-partum and post-partum. The outpatient sent includes ACN clinics, Columbia doctor's private offices, and ultrasound unit.


  • Completion of GCP, HIPPA and applicable regulatory training
  • Complete certification requirements for assigned protocols
  • Screen designated schedules or patient lists for eligible subjects
  • Approach and verify eligibility subjects
  • Enroll and consent eligible subjects
  • Complete research study visits as delineated in assigned protocol and manual of operations set forth by sponsor and supervisor.
  • Complete Telephone follow-up and telephone reminder calls for study participants, during these phone calls the person will need to administer study questionnaire as assigned
  • Coordinate the collection of all research data points as assigned, whether through research visits, chart abstraction or telephone.
  • Scheduling of research visits
  • Collection through venipuncture, processing, tracking, transporting and shipping of biological specimens (including birth specimens) as assigned and by steps delineated in the protocol or manual of operations.
  • Completion study documents and files some examples might include case report forms, worksheets and medical record notes.
  • Maintain confidentiality of documents and files such as HIPPA.
  • Informing relevant clinical staff regarding subject protocol participation.
  • Assist in other research related activities and projects as needed
  • Regular collaboration with the PI and other research staff
  • Participate in on-call activities to cover research activity off- hours.
  • The candidate will perform other related duties as assigned.

Minimum Qualifications

  • Requires a bachelor's degree or equivalent in education and experience, plus three years of related experience.
  • Type minimum qualifications
  • Complete proficiency in written and spoken English and Spanish ( required)
  • Experience in a patient care setting and clinical research experience ( required)
  • Incumbent must be self-directed and able to make independent decision within the parameters of all federal, state, institutional and departmental guidelines.
  • Excellent interpersonal, written/oral communication, and organizational skills are required
  • Proficiency in Microsoft Office

Preferred Qualifications

  • Phlebotomy certificate (preferred to be obtained within 3 months of hire)

Equal Opportunity Employer / Disability / Veteran

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

Applications open: May 17 2021 Eastern Daylight Time Applications close:

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Keywords: Columbia University, New York , Clinical Research Coordinator I, Other , New York, New York

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