Pharmacovigilance Specialist

1 week ago


Cheltenham, Gloucestershire, United Kingdom Pharma Partners Recruitment Ltd Full time
Job Description

Pharma Partners Recruitment Ltd is seeking a highly skilled Pharmacovigilance Specialist to join our team. As a key member of our Medical Affairs department, you will play a crucial role in ensuring the safety of our clients' products.

Key Responsibilities:
  • Safety Data Management: Review and analyze safety data from various sources, including spontaneous reports, literature sources, and regulatory authorities.
  • Literature Review: Conduct systematic reviews of safety information published in the scientific literature, in partnership with third-party service providers.
  • Case Processing: Process and assess Individual Case Safety Reports (ICSRs), including data entry and triage.
  • Signal Management: Detect, assess, and recommend actions for safety signals.
  • Risk Management and Minimization: Develop and maintain Risk Management Plans, and implement risk minimization activities, including product labeling and additional materials.
  • Aggregate Safety Reports: Author, co-author, and review aggregate safety reports (PSURs, PBRERs) with the Medical Affairs team.
  • Product Maintenance and Development: Author safety-related information, including product labeling updates, and coordinate regulatory activities.
Requirements:
  • A degree in Biological or Biomedical Sciences, with a postgraduate degree an advantage.
  • Relevant experience in Pharmacovigilance and Medication/Patient Safety.
  • Clear understanding of current and developing legislation, ethics, and practice, with the ability to apply this to company processes.
  • Outstanding communication and medical writing skills, with exceptional attention to detail.
  • Ability to build and maintain effective working relationships with cross-functional and multi-national colleagues.
  • Ability to meet deadlines while managing multiple responsibilities.
  • Professionalism and integrity.


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