Job Details
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.