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Clinical Research Coordinator (Dublin, OH) in Columbus at Vaco

Date Posted: 5/7/2019

Job Snapshot

Job Description

Vaco has a client in Columbus, OH that is actively seeking a direct-hire Clinical Research Coordinator I.

Summary:
The CRC I is responsible for understanding and implementing clinical studies and trials under the Private Investigator's direction.

Responsibilities:

  • Oversee the full lifecycle of clinical trials from start to finish
  • Liaise between research staff, drug companies, sponsors, and other regulatory agencies
  • Schedule and conduct patient visits as well as FDA audits
  • Conduct trainings on protocols for study staff and explain study updates with all appropriate parties
  • Ensure that informed consent forms are completed according to protocol guidelines
  • Perform vitals, ECG, and other study assessments
  • Collect, process, and ship laboratory samples
  • Record events throughout trial and report to appropriate staff in order to determine timely resolution
  • Maintain regulatory documents from study start up to completion
  • Other responsibilities as needed

Job Requirements

- Bachelor's degree in science, psychology or related field; 4 years of additional relevant experience in lieu of degree • Minimum of 2 years of experience in research required with understanding of medical terminology • Proficient with MS Office, specifically Excel • Self-motivated and able to work with limited supervision • Written and verbal communication skills • Ability to handle multiple priorities and manage time efficiently • Enjoy interfacing with people with an ability to listen and demonstrate understanding • Detail-orientation