Clinical Research Coordinator
Company: Nuvance Health
Posted on: June 12, 2021
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.
Reports to Director of Clinical Trials or Clinical Research
Nurse Lead: 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 Oncology therapeutic areas. 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
Screens patients for study participation e.g. reviews medical
record, collaborates with medical & research staff, etc. and
procures informed consent.
Maintains accurate and thorough documentation on all source
documents and case report forms (CRFs) for each study patient.
Enters data. Resolves all patient queries.
Maintains communication with investigators/researchers,
patients, internal and external collaborators (e.g. consulting
physicians, Monitors), sponsors, federal regulatory agencies, and
other involved parties as required.
Participates in investigator, coordinator, or study initiation
meetings accordingly. Coordinates and participates in monitoring
visits/audits with regulatory agencies or sponsors.
Maintains current regulatory (GCP, HSR) and study specific
Prepares and submits all study protocols, consent forms, and
other required documents to the Institutional Review Board
Educates hospital staff about protocols through in-services,
written materials and one-on-one interaction, for each study and
each patient, and for general marketing.
Demonstrates flexibility in daily routine and effectively
accommodates for the needs of the job (e.g. early or late patient
Performs procedures including EKG, Phlebotomy, blood and body
fluid sampling, packing and shipment of human samples, body
measurements and examinations within scope of practice and
training, consistent with clinic and study specific
policies/procedures and scope of care under the guidance of the
Fulfills all compliance responsibilities related to the
- Performs other duties as assigned.
Location: Danbury-24 Hospital Ave
Work Type: Full-Time
Standard Hours: 40.00
Work Schedule: Day 8
Work Shift: 8:30am-5:00pm
Org Unit: 180
Department: Cancer Research
- Some manual skills / motor coord & finger dexterity
- Sedentary/light effort. May exert up to 10 lbs. force
- Generally pleasant working conditions.
- Some occupational risk
Nuvance Health and its affiliates are Section 501(c)(3)
tax-exempt organizations and therefore eligible employees may
qualify for forgiveness of certain federal student loans under the
Public Service Loan Forgiveness Program.
WE ARE AN EQUAL OPPORTUNITY EMPLOYER. Qualified Applicants are
considered for positions and are evaluated without regard to mental
or physical disability, race, color, religion, gender, national
origin, age, genetic information, military or veteran status,
sexual orientation, marital status or any other classification
protected under applicable Federal, State or Local law.
We will endeavor to make a reasonable accommodation to the known
physical or mental limitations of a qualified applicant with a
disability unless the accommodation would impose an undue hardship
on the operation of our business. If you believe you require such
assistance to complete this form or to participate in an interview,
please contact Human Resources at 203-739-7330 (for reasonable
accommodation requests only). Please provide all information
requested to assure that you are considered for current or future
Keywords: Nuvance Health, Danbury , Clinical Research Coordinator, Other , Danbury, Connecticut
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