Sarah Bly
Worldwide Clinical Trials
Sarah joined Worldwide Clinical Trials in 2005 where she began her career in clinical research as a Data Coordinator, after which she became a Clinical Research Associate. Sarah has been a highly motivated regulatory specialist for over 14 years where she provides strategic senior-level regulatory intelligence direction and planning for the integration of advanced regulatory intelligence, to all teams especially the medical writing team. Sarah drives Worldwide’s implementation of short term and long-term objectives for regulatory intelligence initiatives. Her role includes oversight of expert regulatory intelligence training ahead of new regulations.