Jobs · Analyst · Ohio

Clinical Research Coordinator 2-Neurology

AnalystFull-time

About the role

The Clinical Research Coordinator will coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer College of Medicine (COM) Center for Clinical Research Management (CCRM) for the Department of Neurology/ Division of Cognitive Neurology.

Responsibilities

  • Assesses 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
  • Edits and educates patients and families of purpose, goals, and processes of clinical study
  • Schedules and follows through with patient care appointments, procedures, & other diagnostic testing in accordance with study protocol
  • Collects, processes & evaluates biological samples
  • Administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires
  • Monitors 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
  • Evaluates patients for compliance related to protocol
  • Collects, extracts, codes, and analyzes 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
  • Coordinates and prepares for external quality assurance and control reviews by IRB, federal or industry sponsors
  • Participates in developing new research protocols and contributing to the 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
  • Two to four years of relevant experience preferred
  • Experience or knowledge in cognitive diseases/disorders preferred
  • Knowledge of medical terminology desired
  • Computer skills required with experience using Microsoft Software applications desired
  • Clinical research certification from an accredited certifying agency desired (ACRP or SOCRA)

Qualifications

  • Minimum Education and Skills/Experience Required/Desired: Bachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required. Experience Required: One year experience in a clinical research capacity required. Desired Experience: Two to four years of relevant experience preferred.
  • Desired Certification: Clinical research certification from an accredited certifying agency desired (ACRP or SOCRA).
  • Requires successful completion of a background check.

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