Pharmacovigilance Intern

OpellaMorristown, NJ
1dOnsite

About The Position

We're looking for the best candidates out there who want to make a difference in consumers’ lives. Candidates who have a zest for learning and are ready to make an impact within the pharmaceutical Industry. This person will gather experience by working with US/Canada affiliates on multiple interactions and projects with other business functions. They will also get an opportunity to interact with other Country Safety Heads and QPPV offices to learn about their roles.

Requirements

  • Currently pursuing Bachelor’s degree with focus on healthcare related career (PharmD, B.S/M.S in Biomedical Engineering, Epidemiology, Pharmaceutical Sciences etc.)
  • Demonstrate ability to work in a team environment.
  • Demonstrate ability to think creatively to solve complex problems.
  • Exhibits eagerness to learn and ability to learn quickly.
  • Exceptional written and oral communication skills, and attention to detail
  • Able to multitask, be a self-starter, and collaborate closely with cross functional teams.
  • Intuitive understanding of today's digital and social culture, with fluency in platform usage.
  • Team player with a can-do attitude where no task is too big or small.
  • Ability to effectively prioritize and manage multiple tasks to meet deadlines.
  • Deadline-driven, quick to move and able to develop executional plans in real time.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.

Responsibilities

  • The intern will work with the safety data management team. This team is responsible for supporting Consumer Healthcare’s safety reporting globally by providing high quality and timely safety data outputs and ongoing business configuration of safety systems.
  • Support sorting and clearing data dump from Sanofi Healthcare for worldwide exposure data to be used in PBRERs
  • Support the preparation of certain PV audits scheduled in the 2nd half of the year:.
  • Support PSMF update for the new PV organizational structural change.
  • Support Signal lead to ensure legacy data from Sanofi for signals is validated in the signal tool.
  • Support Risk Management lead in Risk Management SOP reduction work.
  • Candidates must be available 40 hours per week, Monday – Friday during standard business hours in EST.
  • Candidates must be available to participate in a 8-week engagement May – July 2026.
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