Senior/principal Drug Safety Specialist (night Shift)

Thermo Fisher Scientific UK

Remote
**
Collection, monitoring, assessment, evaluation, research, and tracking of safety information
Collaboration with project team members, client contacts, investigators, adverse event reporters, and third-party vendors
Review of regulatory/pharmacovigilance publications
** Thermo Fisher Scientific is seeking a Senior/Principal Drug Safety Specialist for a night shift position, which involves overseeing pharmacovigilance activities in a regulated environment. The role requires strong critical thinking, problem-solving skills, and the ability to manage multiple tasks while ensuring patient safety. **

Job Summary

  • As a Senior Safety Specialist, you'll perform and may oversee day-to-day Pharmacovigilance (PV) activities within a highly regulated environment driven by strict timelines.
  • Your responsibilities will include, but are not limited to, the collection, monitoring, assessment, evaluation, research, and tracking of safety information.
  • You will effectively collaborate with various parties such as project team members, client contacts, investigators, adverse event reporters, and third-party vendors.

Matching Summary

Match Score: 75

** Thermo Fisher Scientific is seeking a Senior/Principal Drug Safety Specialist for a night shift position, which involves overseeing pharmacovigilance activities in a regulated environment. The role requires strong critical thinking, problem-solving skills, and the ability to manage multiple tasks while ensuring patient safety. **

Skills & Requirements

Must-have

  • collection, monitoring, assessment, evaluation, research, and tracking of safety information
  • collaboration with project team members, client contacts, investigators, adverse event reporters, and third-party vendors
  • review of regulatory/pharmacovigilance publications
  • maintains medical understanding of applicable therapeutic area and disease states
  • thorough understanding of global regulatory requirements
  • ability to manage and prioritize a variety of tasks and meet strict deadlines with limited supervision
  • strong attention to detail

Nice-to-have

  • positive and professional demeanor in challenging circumstances
  • work effectively within a team to attain a shared goal

Key Requirements

  • Bachelor's degree or equivalent
  • 5+ years of relevant experience
  • Thorough understanding of pathophysiology and the disease process
  • Strong knowledge of relevant therapeutic areas
  • Excellent critical thinking and problem solving skills
  • Proficient at complex clinical study administration including budget activities and forecasting
  • Excellent oral and written communication skills
  • Good command of English
  • Computer literate with the ability to work within multiple databases
  • Proficient in Microsoft Office products

Work Rights

Not specified

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