Sara N. Frye

Experience

1. Clinical Lead, Clinical Development & Medical Affairs

   Alcon

   Jan 2022 — Present

   Planning, directing, creating and communicating clinical study timelines; gathering input from cross-functional teams and creating plans to produce deliverables on schedule; ensuring consistency of clinical study and processes across clinical trials; overseeing and resolving operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations; preparing clinical trial budgets; ensuring study is conducted within clinical trial protocols; monitoring progress and following up with team members and line managers when issues develop; implementing and preparing the clinical development strategy as outlined by the clinical teams; assisting in the development of recruitment strategy for the trial in program; supporting life cycle management activities for ophthalmic medical devices; providing clinical functional review and expertise on assigned projects; authoring, revising, and updating clinical documents for Medical Device Regulation (MDR) remediation and Post Production Risk Reviews (PPRR).

Education

• Nova Southeastern University

  Doctor of Optometry, Optometry

  2005 — 2009

• University of California, Berkeley

  Optometry Residency, Cornea & Contact Lens

  2009 — 2010

• University of Arizona

  Master of Public Health - MPH, Health Services Administration

  2015 — 2020

• The University of British Columbia

  Bachelor of Science

  2000 — 2004