Liz Farrell

Director, Trial Master File

Liz Farrell is the Director, Trial Master File Process Lead at Agios Pharmaceuticals, responsible for Agios’ TMF and clinical document management strategy and collaborates with cross-functional departments to ensure inspection readiness across the Trial Master File. Liz has been working in the pharmaceutical industry for over 15 years, with a primary focus in TMF as well as Clinical Operations. During this time, she has led the design and implementation of TMF metrics programs, implemented several global eTMF systems, managed TMF migrations both from CRO to Sponsor, as well as between in-house eTMF systems, and managed TMF Leads and Study Owner teams. She has also participated in numerous regulatory authority inspections (FDA, MHRA, PMDA, Health Canada) as the TMF SME. Prior to her position at Agios, Liz managed TMF Process at Biogen, held several Clinical Operations roles at small pharma companies, and performed clinical research at Vanderbilt University Medical Center.

speaker Agenda

Speaker Sessions

hours of fun

Register for the worlds largest TMF event

Complete the short form below to register for FREE. All fields indicated with an * are required.

🎉 Congratulations 🎉

You're now registered for TMF Week 2023!

You 'll now receive an email confirming your registration with steps on what to do next. If you don't receive an email please email us at marketing@montrium.com

Oops! Something went wrong.

Posts by 

Liz Farrell

No items found.

Join thousands of other ClinOps professionals from around the world