Clinical Research Coordinator

• Must be phlebotomy trained.
• Identify and recruit eligible participants.
• Conduct pre-screening interviews to ensure candidates meet study criteria.
• Maintain sponsor provided prescreening logs.
• Maintain appropriate Elevate portals with pertinent information.
  

Maintain accurate data collection and maintain databases.

• Ensure data integrity throughout the study.
• Abide by all ALCOA principles.
  
  

Serve as a point of contact for participants, providing information about the study

and addressing concerns.

• Conduct informed consent processes and review participants' medical histories.
• Complete delegated study procedures within local and state regulations