Clinical Research Coordinator

Clinical Research Coordinator (Onsite - Middletown, NJ)

This is a 3-6+ month assignment

Assignment Overview:

Our client is an innovative medical device manufacturer who is committed to delivering life-changing therapies for patients around the globe. Our client needs a Clinical Research Coordinator to support one of their leading clinical sites with prospective and retrospective Clinical Research studies. This assignment offers clinical professionals an opportunity to work on an innovative product.

Primary Responsibilities:

• Ensure the client’s study is compliance with local and federal laws and regulations.
• Recruit and screen potential study participants
• Performs intake assessments
• Create and/or maintain all documents and records related to the study
• Conduct informed consent process as delegated by the investigator and in compliance with IRB oversight and principle of Good Clinical Practice (GCP).
• Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress.
• Manage the inventory of equipment and supplies related to the study as needed
• Collect data and patient information into electronic systems, for prospective and retrospective clinical studies.
• Create reports on each study, including notes on protocols, workload, data collection, etc.

Technical Requirements

• 1-2+ years of experience working in as a Clinical Research Coordinator (medical device preferred, but at least some pharmaceutical or biotechnology if no device experience)
• Bachelor’s Degree in a scientific discipline
• Working knowledge and understanding of principles of GCP and appropriate FDA regulations related to Clinical Research.
• Experience with Class III medical devices

Job Type: Contract

Pay: $33.00 - $38.00 per hour

Schedule:

• 8 hour shift

Ability to Relocate:

• Middletown, NJ: Relocate before starting work (Required)

Work Location: In person