Rachael Cavanagh

Rachael is a regulatory affairs professional, with 12+ years’ experience in pharmaceutical and medical device regulatory affairs.

Prior to joining tranScrip, Rachael worked both in industry and at CROs with experience preparing and submitting regulatory packages, project management of regulatory submissions and regulatory strategy.  She has experience managing large product portfolios and team members.

Her experience is global, with a strong emphasis on European regions; with submission work ranging from clinical trials, marketing authorisation applications and post-marketing activities.

Rachael has a Bachelor of Science degree (Hons) in Pharmaceutical Sciences and Clinical Research from Liverpool John Moores University.