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.