Joanna Paul, PhD

Regulatory Affairs Practice – Europe

OVERVIEW

FOCUS AREAS

More than 15 years experience as a medical writer

Clinical Study Reports
Module 2.7.3 and module 2.7.4 summary documents
Plain language writing

As medical writing manager, Jo writes and develops documentation for interactions with regulatory authorities.

Jo has 15+ years experience as a medical writer in both large pharma and contract research organisations. Jo has worked across clinical development phases and therapeutic areas to produce documents for a global audience. Jo can effectively summarise complex information into key messages to create cohesive and readable documents. Jo is experienced at working with complex clinical data and extracting key messages.

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