Beth Fehrle

About Beth Fehrle

With more than 20 years of experience in the pharmaceutical industry, I am Director, Operations at MMS – a global, leading clinical research organization. On a daily basis, I work with the global team members to ensure outstanding services that meet regulatory requirements and high-quality standards.Prior to my tenure at MMS, I spent over 15 years at Pfizer where I led the regulatory operations team supporting global regulatory submissions across many therapeutic areas and indications as Associate Director.As a leader, I am a focused on encouraging the skills and strength of each individual that contribute to our exceptional high-quality services.

Experience

1. Director, Operations

   MMS

   Jan 2022 — Present

   Provides oversight and coordination of operational projects and activities with a focus to improve efficiency, increase communication and streamline processes. Appointed to the Company’s Innovation Leadership Team in the January 2022.

Education

• Baker College

  MBA, Business Administration and Management

  2001 — 2005

• Eastern Michigan University

  Bachelor's of Science

  1984 — 1988

Skills

• Biotechnology
• Oncology
• Protocol
• Medical Devices
• Clinical Trials
• Clinical Development
• U.s. Title 21 Cfr Part 11 Regulation
• Regulatory Requirements
• Electronic Data Capture (Edc)
• Pharmaceutical Industry
• Communication
• CRO
• Regulatory Affairs
• Medical Writing
• Edc
• Ctms
• Pharmaceutics
• Drug Discovery
• Clinical Trial Management System (Ctms)
• Regulatory Submissions
• 21 Cfr Part 11
• Drug Development