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Senior Clinical Research Coordinator

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

Job Description:

  • Requisition no: 503172
  • Work type: Full Time
  • Location: Other US Locations, Medical Center
  • School/Department: Herbert Irving Comprehensive Cancer Center
  • Grade: Grade 104
  • Categories: General Administration
  • Job Type: Officer of Administration
  • Regular/Temporary: Regular
  • Hours Per Week: 35

Position Summary

The Senior Clinical Research Coordinator (sCRC) within the Herbert Irving Comprehensive Cancer Center (HICCC) will work with the Clinical Research Manager and Clinical Research Team to manage data associated with clinical trials involving human subject research.

Supervise clinical trials and clinical research coordinators within the Herbert Irving Comprehensive Cancer Center. This position reports directly to the Clinical Research Manager of the specific disease site this incumbent is assigned to.

Responsibilities

The Senior Clinical Research Coordinator (sCRC) will play an integral role in the coordination and conduct of clinical trials involving human subject research. In addition, this position includes all the duties of the Senior Clinical Research Coordinator as well as the following responsibilities:

  • Assist in the proper execution of the clinical research protocols; the prioritization and coordination of daily routines to ensure proper execution of clinical research protocols, informed consent, follow-up procedures and case report forms are completed.

  • Coordination of clinical research protocols; timely and appropriate interaction with sponsors, data coordinating centers and core laboratory personnel as needed.

  • Help arrange and participate in Investigator meetings and site initiation visit.

  • Work closely with the regulatory team to ensure timely submission or new protocols, renewal, modifications and other regulatory functions.

  • Maintain patient confidentiality and will ensure that pertinent tests, procedures and lab work are completed in a timely and confidential manor.

  • Patient registration and data entry in the Herbert Irving Comprehensive Cancer Center's central patient database called Velos.

  • Practice GCP and FDA/HHS regulations and will comply with Columbia University and Hospital policies and procedures related to Clinical Research. The incumbent will collect data and complete case report forms appropriately.

  • Education, training and ongoing supervision of pertinent staff members about the protocol(s).

  • Participation in committee or other meetings as assigned.

  • Coordinator will also perform other related duties as assigned.

Minimum Qualifications

  • Requires a bachelor's degree or equivalent in education, training and experience plus 3 years of related experience.

Preferred Qualifications

  • Master's degree in management or public health is preferable

Other Requirements

  • Excellent interpersonal and organizational skills
  • 2 years of Oncology Clinical trials experience
  • Excellent interpersonal and organizational skills
  • Computer Skills: proficiency with MS Word programs and familiarity with Mac and PC platforms

Equal Opportunity Employer / Disability / Veteran

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

Applications open: Feb 05 2021 Eastern Standard Time Applications close:

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

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