Job Description
At-a-Glance:
Are you ready to build your career by joining a healthcare provider? If so, our client is hiring a Clinical Research Coordinator.
Position Type:
Contract
Hybrid (3 DAYS ONSITE, FLEXIBLE ON WHICH DAYS)
Required: Duration: 13 weeks
Onsite or Remote: HYBRID - 3 DAYS ONSITE, FLEXIBLE ON WHICH DAYS
Shift: 5X8 0800-1600
Clinical Research Coordinator experience Require
Responsibilities: Required Skills: Create and maintain study flows
informed consent facilitation
Maintain Accurate and Complete Subject Records
Protocol Compliance
Subject Enrollment Form
IRB Compliance
Principal Investigator Responsibilities
Proficient EMR navigation
Preferred Skills: Experience in an ONC setting preferred
Experience with Phase II and III preferred
Experience with venipuncture/phleb preferred
Experience with Patient Enrollment preferred
IRB Submission
Maintain Accurate and Complete Regulatory Records
Setup study files (FDA 1572, Collection of CVs)
Site Visit Log
Telephone Log
Test Article Inventory System and Drug Accountability
Sponsor Obligations
Understanding of Query Process
Clinical Documentation guidelines
Get in Touch:
We want to hear from you! If you think you'd be a good match, submit your resume and reach out to Somya at 201-366-0756 to learn more. Hired by Matrix
Job Tags
Contract work, Flexible hours, Shift work,
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