Research Coord/Sonographer

Sarasota Memorial Health Care SystemSarasota, FL
Onsite

About The Position

This position is responsible for preparing and submitting regulatory submissions to the IRB and sponsors, ensuring documentation compliance for multiple study projects, audit preparation, and data submission. The role involves advising patients on trial design, facilitating informed consent for investigators, strictly adhering to protocol procedures for each study, screening for potential trial patients based on eligibility criteria, and managing patient follow-up. The position is responsible for the coordination of these trial activities, among others.

Requirements

  • Graduation from a Cardiovascular Technology Program.
  • Completion of Good Clinical Practice, Human Subject Protection, and Safe Handling/Hazardous training programs within thirty (30) days of hire.
  • A minimum of five (5) years of healthcare experience, preferably with previous pertinent cardiovascular sonography experience.
  • Cardiac sonography and vascular specialty credentialing from: Registered Diagnostic Cardiac Sonographer (RDCS) and Registered Vascular Technologist (RVT) certifications by the American Registry for Diagnostic Medical Sonography (ARDMS) OR Registered Congenital Cardiac Sonographer (RCCS) or Registered Cardiac Sonographer (RCS), and Registered Vascular Specialist (RVS) certification by Cardiovascular Credentialing International (CCI). Credentials can be a combination of the above.

Nice To Haves

  • An organized individual with strong critical thinking skills who can work efficiently under pressure.
  • In-depth knowledge of good clinical practices as set forth by Federal regulations.
  • Someone who is highly motivated, shows initiative, is proactive, and able to work independently, as well as, on a team.
  • Prior research experience either in formal or informal capacity.

Responsibilities

  • Prepares and submits regulatory submission to IRB and sponsors.
  • Ensures documentation compliance for multiple study projects.
  • Prepares for audits.
  • Manages data submission.
  • Advises patients of trial design.
  • Facilitates informed consent for investigators.
  • Follows strict adherence to protocol procedures specific to each study.
  • Screens for possible trial patients and eligibility criteria.
  • Manages patient follow-up.
  • Coordinates trial activities.
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