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Clinical Research Coordinator
Opening : Clinical Research Coordinator
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 its done correctly.
- 3-5 years 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. 1.3 Ensures all appropriate subject consents are obtained.
1.4 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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