Too often, individuals aspiring to become Clinical Research Associates (e.g., Study Coordinators) don’t have the required means to learn about this crucial role. Moreover, new CRAs are often sent into their earliest site monitoring visits with limited practical training or oversight, and with little appreciation for the best practices of veterans in the field. This hands-on workshop is designed to give practical tools and tips on conducting a monitoring visit, fill gaps in basic monitoring knowledge, give an opportunity to practice monitoring scenarios, and provide a judgement-free environment for asking the questions that new CRAs often hesitate to raise with their managers and Study Coordinators struggle to find answers for.

CEU: 2.00 ACRP

Speakers:

• Demi MacLennan, MS, CCRA, ACRP-PM, Sr. Project Manager, Fortrea

• Negar Roofigari, Clinical Trial Manager, Fortrea

Watch Sneak Peeks into the Session Content: