Liz Farrell

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.