Overall Role

Recruit, screen, and consent research participants; schedule and conduct research visits with participants remotely and in-person; collect specimens and monitor participants; and input data into electronic data capture systems. Create and update standard operating procedures, manage study data, and generate reports. Assist with the creation of posters, manuscripts, and presentations for scientific meetings and/or grant submissions and be responsible for preparing IRB applications, amendments, scheduled continuing reviews, and adverse event reports

Job Functions

  • Coordinate Research Studies
  • Crate and Manage Standard Operating Procedures
  • Creation of Posters, Manuscripts and Presentations
  • Manage Regulatory and Reporting Documentation
  • COP Research Study Team Member Backup