CV / English / Pharmacovigilance Scientist

Personal Information

  • Name: Daniel Sterling
  • Address: 485 Sunshine Ave, Medville, CA 23456
  • Email: [email protected]
  • Phone: (555) 123-4567

Professional Profile

A dedicated and detail-oriented Pharmacovigilance Scientist with over 5 years of experience in the pharmaceutical industry. Skilled at assessing and reporting on the safety profiles of pharmaceutical products, with a strong foundation in both pre- and post-market drug safety studies. Adept at working with cross-functional teams to monitor, evaluate, and ensure compliance with global regulatory standards.

Core Competencies

  • Drug Safety and Pharmacovigilance
  • Regulatory Compliance
  • Adverse Event Reporting Systems (AERS)
  • Risk Management
  • Clinical Trial Monitoring
  • Data Analysis & Reporting
  • Cross-functional Team Collaboration

Technologies & Certifications

  • Certifications: Certified Drug Safety Specialist (CDSS)
  • Software Proficiency: Argus Database, Veeva Vault Safety, Microsoft Office Suite
  • Data Analysis Tools: SAS, SPSS

Professional Experience

Senior Pharmacovigilance Scientist, NexPharma Inc., Medville, CA

April 2019 - Present

  • Led a team to implement new drug safety monitoring protocols, which reduced adverse event report processing time by 30%.
  • Collaborated with regulatory affairs to ensure compliance with FDA and EMA guidelines for pharmacovigilance.
  • Played a key role in the post-market surveillance of three major drug releases, identifying critical safety concerns that led to swift regulatory action.

Pharmacovigilance Associate, WellPharm Co., San Francisco, CA

July 2017 - March 2019

  • Analyzed and processed over 10,000 adverse event reports, improving data accuracy by 25%.
  • Assisted in the development of risk management plans for several high-profile drug launches.
  • Coordinated with research teams to facilitate phase IV clinical trials, ensuring optimal patient safety.

Education & Training

  • M.S. in Pharmacy, Focus on Pharmacovigilance & Drug Safety University of California, San Francisco, 2017

  • B.S. in Biological Sciences University of California, Davis, 2015

Referees

Dr. Emily Hartwell Senior Research Scientist, NexPharma Inc. Email: [email protected] Phone: (555) 234-5678

Mr. Thomas Guerrero Director of Regulatory Affairs, WellPharm Co. Email: [email protected] Phone: (555) 345-6789