HealthQuest

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Clinical Research Coordinator

at HealthQuest

Posted: 10/4/2019
Job Reference #: 17693

Job Description

  • Job LocationUS-NY-Poughkeepsie
    Posted Date2 months ago(8/8/2019 10:31 AM)
    Requisition #
    24393
    Type
    Full Time
    Primary Shift
    Day
    Hours Per Week
    40.00
  • Overview

    Nuvance Health is a family of award-winning nonprofit hospitals and healthcare professionals in the Hudson Valley and western Connecticut. Nuvance Health combines highly skilled physicians, state-of-the-art facilities and technology, and compassionate caregivers dedicated to providing quality care across a variety of clinical areas, including Cardiovascular, Neurosciences, Oncology, Orthopedics, and Primary Care.

    Nuvance Health has a network of convenient hospital and outpatient locations — Danbury Hospital, New Milford Hospital, Norwalk Hospital and Sharon Hospital in Connecticut, and Northern Dutchess Hospital, Putnam Hospital Center and Vassar Brothers Medical Center in New York — plus multiple primary and specialty care physician practices locations, including The Heart Center, a leading provider of cardiology care, and two urgent care offices. Non-acute care is offered through various affiliates, including the Thompson House for rehabilitation and skilled nursing services, and the Home Care organizations. For more information about Nuvance Health, visit www.nuvancehealth.org.

    Responsibilities

    The Clinical Research Coordinator coordinates clinical research activities within the research division through the use of Good Clinical Practice Guidelines.

    Function independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporations.
    Facilitates and coordinates the daily clinical trial activities and plays a criticial role in the conduct of Reads and understands research protocols and serves as a resource person to physicians, Medical Center staff, and the community.
    Acts as liaison between sponsor and potential investigator before and during the site selection process by arranging site visit with sponsor, preparing supporting documentation for site visit, and facilitating sponsor on the day of the visit.
    Ensures the completion of required study forms in a timely manner, responds to data clarification requests in a timely manner.

    Qualifications

    Education and Experience Requirements:

    BA/BS required – OR - allied health professional degree – OR - HS diploma with CRC Certification
    Minimum three (3) years’ experience in health care with one year of clinical research practice preferred.
    BLS preferred or obtain after employment
    Working knowledge of health care, including treatment, patient care, diagnosis and follow-up
    Minimum Knowledge, Skills and Abilities Requirements:

    MS Excel, Windows, PowerPoint.
    Proven ability to work independently.
    License, Registration, or Certification Requirements:

    CCRC or CCRP preferred. If not current, candidate to obtain within 2 years