Full-Time

Senior Clinical Research Coordinator

Confirmed live in the last 24 hours

Ohio State University - Columbus

Ohio State University - Columbus

No salary listed

Senior

Company Does Not Provide H1B Sponsorship

Columbus, OH, USA

Position is located at The Ohio State University, Columbus campus.

Category
Public Health
Biology & Biotech
Required Skills
Data Analysis
Requirements
  • Bachelor’s Degree in biological sciences, health sciences or medical field or an equivalent combination of education and experience required
  • Three to five years’ experience in a clinical research capacity conducting clinical research studies required
  • Clinical research certification from an accredited certifying agency required (SOCRA or ACRP) and must be maintained
Responsibilities
  • Serves as lead resource in the execution of assigned clinical research studies in accordance with approved protocols
  • Oversees, implements & coordinates conduct of daily activities of research studies
  • Recruits, interviews and promotes study to eligible participants
  • Educates participants and families of purpose, goals, and processes of clinical study
  • Leads participant enrollment activities and ensures informed consent authorization is obtained & administered in compliance to regulatory & sponsor requirements
  • Facilitates collection, processing & evaluation of biological samples, as well as scheduling and follow-through of study visits, procedures, & other testing
  • Monitors participants for adverse reactions to study procedures and notifies appropriate clinical professional to evaluate participant response, identify status of complications, & provide appropriate level of care
  • Documents unfavorable responses and notifies research sponsors & applicable regulatory agencies
  • Participates in collecting, extracting, coding, and analyzing clinical research data
  • Assists with activities to ensure compliance with Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations
  • Participates in planning, organizing and preparing for external compliance and quality assurance and control reviews
  • Actively participates in internal quality assurance audits
  • Participates in development of new research protocols and contributes to planning of goals to meet study requirements
  • Assists with preparation and submission of publications, research reports, and grant proposals
Desired Qualifications
  • Experience in a progressively independent management capacity in a medical research environment preferred
  • Experience or knowledge in psychiatry/behavioral health and imaging clinical research preferred
  • Computer skills required with experience using Microsoft Software applications desired
Ohio State University - Columbus

Ohio State University - Columbus

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