Health Quest Systems, Inc.

Clinical Research Coordinator

Job Location US-NY-Poughkeepsie
Posted Date 6 months ago(4/21/2020 3:34 PM)
Requisition #
25744
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

Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Responsibilities include; patient screening and recruitment, coordination of care of the research patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board (IRB). Coordinates studies in varied therapeutic areas including but not limited to Cardiovascular, Pulmonary, Gastroenterology, Neurology, Endocrinology, Dermatology and Rheumatology. Functions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporations.

Qualifications

Education and Experience Requirements:

 

Bachelor’s Degree, Allied health professional degree, or equivalent experience.

  • Minimum of one-two (1-2) years’ experience with EDC and CRFs.
  • Minimum Knowledge, Skills and Abilities Requirements:Ability to multi-task and work as a team and independently.
  • Knowledge of Medical Terminology, good clinical practice, FDA, OHRP, and HIPAA policies. 
  • Outstanding interpersonal communication skills.
  • Strong attention to detail, self-motivation, and good organizational skills.
  • Ability to prioritize quickly and follow directions and protocol.
  • License, Registration, or Certification Requirements:
  • Basic Life Support (BLS) certified or willing to obtain upon employment.Valid driver’s license and reliable transportation.PREFER: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or certified within 2 years.
  • Environmental Factors:
  • Bio-hazardous Waste Chemicals/Commercial Products Exposure to LatexInteracting with a Diverse population Patient Care/Handling Duties Risk of Electrical Shock
  • Physical & Mental Requirements:  
  • Repetitive Motion
  • Noise Level – Varies from Quiet to Very Loud
  • Fumes or Airborne Particles
  • Experiencing challenging conditions where a professional attitude will be required
  • Blood Borne Pathogens. Job may require performance or tasks that involve potential for exposure to blood, body fluids, or tissues.
  • Factors affecting environment conditions may vary depending on the assigned work area and tasks

Options

Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
Share on your newsfeed