Full-Time

Clinical Research Coordinator

Confirmed live in the last 24 hours

Ohio State University - Columbus

Ohio State University - Columbus

No salary listed

Junior

Company Does Not Provide H1B Sponsorship

Columbus, OH, USA

Travel locally to OSUWMC outpatient facilities including Outpatient Dublin, New Albany, and East Hospital.

Category
Public Health
Biology & Biotech
Required Skills
Data Analysis
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.
Responsibilities
  • Coordinate and perform daily clinical research activities in accordance with approved protocols.
  • Assist with assessing patient records to identify eligible patients for clinical research protocols.
  • Recruit, interview, and enroll patients.
  • Obtain informed consent and ensure compliance with regulatory and sponsor requirements.
  • Educate patients and families about the purpose, goals, and processes of clinical studies.
  • Coordinate scheduling and follow-through of patient care appointments, procedures, and other diagnostic testing.
  • Participate in the collection, processing, and evaluation of biological samples.
  • Administer, evaluate, and calculate standardized scoring of diagnostic, psychological, or behavioral testing or questionnaires.
  • Assist with monitoring patients for adverse reactions to study treatment, procedure, or medication.
  • Document unfavorable responses and notify research sponsors and applicable regulatory agencies.
  • Participate in evaluating patients for compliance related to protocol.
  • Assist with collecting, extracting, coding, and analyzing clinical research data.
  • Generate reports and reviews to ensure validity of data.
  • Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA, federal, state, and industry sponsor regulations.
  • Assist with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors.
  • Participate in activities to develop new research protocols and contribute to the establishment of study goals to meet protocol requirements.
Desired Qualifications
  • Experience or knowledge in clinical research processes and procedures 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.
Ohio State University - Columbus

Ohio State University - Columbus

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