Miri Alon

About Miri Alon

Over 20 years of experience in the pharmaceutical marketplace, inc. 15 years of drug safety and clinical research.• Knowledge of FDA regulations with a strong scientific background (BS Pharmacy/MHA) and certificates in Clinical Trials Management and Design and Regulatory Affairs.• Extensive knowledge of: ARGUS, ARISg, Medidata RAVE, Covance• RAPS, ACRP and ISPE active member.Specialties: Drug safety, Pharmacovigilance, Medical writing, Clinical Trials oversight, CRO management, Cost-benefit analysis, Risk benefit analysis, Clinical Trials Management and Design & Regulatory affairs certificate

Experience

1. Sr Director, Pharmacovigilance Sciences

   Arvinas

   Dec 2025 — Present

Education

• Tel Aviv University

  M.H.A., Master of Health Administration

  2001 — 2003

• University of California, Santa Cruz

  Certificates:, 1. Clinical Trials Design and Management 2. Regulatory Affairs

  2008 — 2008

• The Hebrew University of Jerusalem

  B.Pharm., Bachelor of Pharmacy

  1995 — 1999

Skills

• Corrective and Preventive Action (Capa)
• Data Management
• Clinical Operations
• Clinical Development
• Gcp
• Regulatory Affairs
• Lifesciences
• Pharmaceutical Industry
• Sop
• Fda
• Drug Safety
• Meddra
• Therapeutic Areas
• Pharmacology
• Electronic Data Capture (Edc)
• Pharmacovigilance
• Quality Control
• Gmp
• Hematology
• Biotechnology
• Pharmaceutics
• Oncology
• Protocol
• Pharmacists
• Ind
• CRO Management
• Clinical Research
• Electronic Medical Record (Emr)
• Clinical Trials
• Clinical Trial Management System (Ctms)
• Healthcare
• Hplc