Clinical Research Coordinator

2 weeks ago


Phoenix, United States Medasource Full time

Opening: Clinical Research Coordinator

Start Date: 5/20

Contract: 6-month contract to hire

Location: Onsite (Phoenix AZ).


Hard Requirements:

  • Investigator Initiated Trial experience
  • Being able to interpret protocol and ensure that it is done correctly.
  • 3-5 years of experience minimum with clinical trials.


Responsibilities:

  • Coordinates and schedules subject study visits to ensure adequate supplies, procedures and investigator availability.
  • Provides study specific, individualized education to study subjects and families.
  • Ensures all appropriate subject consents are obtained.
  • Collects and processes protocol required specimens.
  • Acts as a liaison between Sponsor, Investigator, and Study Subject
  • Collects all required study data and completes CRFs in a timely, accurate manner.
  • Ensures study documents are maintained in compliance with applicable regulations, guidelines, and policies (i.e. FDA, OHRP, IRB)
  • Collaborates with Investigator to identify adverse events/ serious adverse events to ensure study subject safety and accurate and timely reporting.
  • Ensures appropriate internal and external customer service by demonstrating professional interactions with Sponsor, study monitors, and other departments.
  • Complies with all regulatory and policy requirements.
  • Demonstrates knowledge of federal and state regulations, guidelines, and policies governing the conduct of clinical trials.



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