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Tuesday, June 25 • 10:30am - 11:30am
#239: Improving Clinical Trial Risk Management: How To Leverage the IRB's Designed Purpose

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Component Type: Session
CE: ACPE 1.00 Application UAN: 0286-0000-19-598-L04-P; CME 1.00; IACET 1.00; RN 1.00


Approach to Advancing Proactive Quality Through the Implementation of an Integrated Quality Risk Management Framework
Fidelle Jarmon, MS

CRO Perspective
Ben Quartley, PhD


Fidelle Jarmon

Director, Risk Management, Bioresearch Quality and Compliance, Janssen
Fidelle has been with Johnson & Johnson for 10 years. She is currently the Director of Risk Management in the Bioresearch Quality & Compliance organization at Janssen. She is responsible for the further development, implementation, and continuous improvement of the Integrated Risk... Read More →
avatar for Ben Quartley

Ben Quartley

Head of Feasibility, Patient Recruitment and Engagement, Covance
Ben has spent more than 20 years in the Pharmaceutical Industry and has broad experience in Project management and Clinical Operations, having worked at a Site Management Organization, large Pharma and CROs. Early in his career he saw the challenges of accurately planning and delivering... Read More →

Tuesday June 25, 2019 10:30am - 11:30am PDT
Room 17AB San Diego Convention Center 111 W Harbor Drive, San Diego, CA 92101 USA
  08: R-D Quality-Compliance, Session