Job Description

Job Description

Highlights

• $33 - $38/hr based on experience
• Great benefits including 401k w/match and 15 days PTO
• Consistent schedule, no overnights or weekends
• Work with Phase I - III cardiovascular and metabolic studies!

• About Our Client

  Our client is a fast growing site network that currently has over 35 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors.

  Responsibilities

  As a CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process!

  • Conduct procedures such as vital signs, blood draws, EKGs, and bladder scans.
  • Patient recruitment, enrollment, scheduling, and consent
  • Lab procedures and shipments
  • Maintain GCP and follow protocols
  • Data management in EDC systems
  • Overall coordination of the study

  Qualifications:

  • 2+ years of experience working as a CRC on sponsor backed clinical trials
  • Phlebotomy and lab processing experience (ability to perform without supervision)
  • Ability to work on site M-F on site (there is no remote or hybrid days)

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