Freddy Byrth

About Freddy Byrth

Thank you for viewing my profile. e-mail: f•••••@gmail.com: I am a senior-level pharmaceutical research professional. My experience includes the operational delivery of phases 1-4 global Clinical Research programs, strategic operations planning, and business leadership of global, multidisciplinary teams. I have a proven ability to lead/manage change and to motivate teams to deliver exceptional performance. Extensive experience in both line management and project management has enabled me to establish a track record of leading/motivating teams to deliver projects on or ahead of schedule and on budget in a dynamic, global environment. My experience in global, interdepartmental, and corporate-level negotiations has given me a strong understanding of and ability to incorporate organizational considerations into strategic and operational decisions. I have been able to create, embrace, and use new ideas and new technologies to meet business needs and build business opportunities. My budget responsibilities have, at times, exceeded $40 million per year ($700 million for the life of the program) in global external spending.BUSINESS AREA EXPERTISEGlobal Clinical OperationsMulti-disciplinary Team LeadershipGlobal Program/Project ManagementLarge-Scale International Vendor ManagementDepartment-level Line ManagementLine Management of Office-Based and Remote EmployeesClinical Research, PhII to PhIVCross-cultural Negotiations I can be reached via LinkedIn and e-mail: f•••••@gmail.com

Experience

1. Global Clinical Operations Consultant

   Glsa Global Life Sciences Alliance

   Jul 2025 — Present · Raleigh-Durham-Chapel Hill, NC, US

Education

• The University of North Carolina at Chapel Hill

  Bachelor's degree, Biology, General

Skills

• Neurology
• Clinical Monitoring
• Dermatology
• Pharmaceuticals
• Clinical Development
• Asthma
• Regulatory Affairs
• Lifesciences
• Life Sciences
• Program Management
• Strategy
• U.s. Title 21 Cfr Part 11 Regulation
• Pharmacovigilance
• Project Management
• Pharmaceutical Industry
• Fda
• U.s. Food and Drug Administration (Fda)
• Clinical Study Design
• Regulatory Submissions
• Leadership
• Clinical Trial Management
• Clinical Research
• Strategic Planning
• Line Management
• Clinical Data Management
• Pharmaceutics
• Vaccines
• Cross-Functional Team Leadership
• CRO
• Ich-Gcp
• R&D
• CRO Management
• Medical Affairs
• Edc
• Therapeutic Areas
• Clinical Trials
• Pharmacology
• Ctms
• Drug Development
• Vendor Management