Clinical Research Coordinator- Neurology

The Ohio State University
1dOnsite

About The Position

Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Center for Clinical Research Management for the Huntington's Clinical Research Division in the Department of Neurology; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with study protocol; participates in the collection, processing & evaluation of biological samples; administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires; assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & provide appropriate level of care; documents unfavorable responses and notifies research sponsors & applicable regulatory agencies; participates in evaluating patients for compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data; generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements.

Requirements

  • Bachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required
  • One year experience in a clinical research capacity required
  • Requires successful completion of a background check

Nice To Haves

  • Experience or knowledge in neurological diseases and disorders preferred
  • Knowledge of medical terminology desired
  • Clinical research certification from an accredited certifying agency desired
  • Computer skills required with experience using Microsoft Software applications desired

Responsibilities

  • Coordinate and perform daily clinical research activities in accordance with approved protocols
  • Assist with assessing patient records to identify eligible patients
  • Recruit, interview, and enroll patients
  • Obtain informed consent
  • Educate patients and families about the study
  • Coordinate patient care appointments and diagnostic testing
  • Participate in the collection, processing, and evaluation of biological samples
  • Administer and evaluate diagnostic, psychological, or behavioral testing
  • Assist with monitoring patients for adverse reactions
  • Document unfavorable responses and notify research sponsors and regulatory agencies
  • Evaluate patients for compliance related to protocol
  • Assist with collecting, extracting, coding, and analyzing clinical research data
  • Generate reports and reviews to ensure data validity
  • Support activities to ensure compliance with IRB, FDA, and other regulations
  • Assist with coordinating and preparing for external quality assurance reviews
  • Participate in activities to develop new research protocols

Benefits

  • Medical, dental and vision coverage, with Ohio State paying a significant portion of the cost.
  • Paid time off, including sick and vacation time and 11 holidays.
  • State retirement plan or an alternative retirement plan, both with generous employer contributions.
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