Increase efficiencies and productivity by automating core reporting tasks for medical writing.
Automate core regulatory report documents across the CTD pyramid and dramatically accelerate submission timelines.
Head of Medical Writing
Jenni is Head of Medical Writing at Yseop, bridging the gap between traditional medical writing and intelligent automation. She helps develop and deploy the solutions that are transforming how our industry creates regulatory documentation.
Jenni’s career began in 2003 following her PhD in Chemistry, initially producing antibody-drug conjugate therapies before becoming an analytical lab head at Novartis. There, she specialized in Chemistry, Manufacturing, and Controls (CMC) and contributed to critical Module 3 regulatory filings. She later transitioned to clinical regulatory writing, where she supported submissions across 14 countries for 14 different pharmaceutical companies, including Module 1, Module 2, Module 5, and more.
To date, Jenni has led or supported over 300 regulatory documents. She has contributed 37 publications and presentations to the field, with 13 of those focusing on the practical application of AI, and is a frequent speaker at AMWA Conferences.
Outside of work, her hobbies include learning French, attending symphony concerts, leading a book club, and playing LEGO with her sons.