Senior Clinical Research Coordinator - Ccc | Clinical Trials Office

The Ohio State University

Remote, , US
**
Clinical research studies execution
Protocol adherence
Informed consent administration
** The Ohio State University is seeking a Senior Clinical Research Coordinator to oversee and coordinate clinical research studies remotely. The ideal candidate will have a background in biological or health sciences, clinical research experience, and relevant certification. **

Job Summary

  • Senior Clinical Research Coordinator serves as lead resource in the execution of assigned clinical research studies in accordance with approved protocols administered by the Clinical Trials Office (CTO) Multi-Center Trial Program (MCTP).
  • Oversees & coordinates conduct of daily activities of research studies; serves as primary reviewer of subsite patient records to assess and identify patients who meet criteria for participation in research studies.
  • Ensures informed consent authorization is obtained & administered in compliance to regulatory & sponsor requirements; oversees the collection, processing & evaluation of biological samples, as well as follow-through of patient care appointments, procedures, & other diagnostic testing.

Matching Summary

Match Score: 75

** The Ohio State University is seeking a Senior Clinical Research Coordinator to oversee and coordinate clinical research studies remotely. The ideal candidate will have a background in biological or health sciences, clinical research experience, and relevant certification. **

Skills & Requirements

Must-have

  • clinical research studies execution
  • protocol adherence
  • informed consent administration
  • biological sample management
  • adverse reaction monitoring
  • regulatory compliance
  • data extraction and analysis

Nice-to-have

  • progressively responsible management experience
  • specialty area knowledge
  • publication preparation
  • grant proposal assistance

Key Requirements

  • Bachelor’s Degree in biological sciences, health sciences or medical field or equivalent
  • three to five years experience in clinical research
  • clinical research certification

Work Rights

Not specified

Tailored Resume

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