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Pharmacovigilance & Technical Services Vet

Life Sciences & Health Care - Pharmaceutical - Safety - Professional Master

Our client a global leader is one of the 15 largest companies in Pharmaceutical industry as well as one of the most reputable companies worldwide.

Feel free to contact

Jeff Sondek, Account manager

Apply now

About this role

• Support key Pharmacovigilance (PV) activities (e.g. data entry, case review and individual/aggregate reporting; trend analysis, signal detection and risk communication);
• Train employees on general reporting responsibilities, including PEI and vendors, as needed. • Interact with internal and external customers with the goal of understanding and meeting their needs.
• Serve as primary contact with Canadian regulatory authorities (CAB/FAB/Aqua). • Review qualifying third party contracts to ensure compliance with internal and external PV requirements.
• Review study protocols to ensure inclusion of a system for timely collection and handling of safety information. • Coordinate Aqua ADE communication with Aqua Health colleagues.
• Drive complex discussions with external or internal customers to collect or clarify key findings. • Support and defend company products through accumulation and interpretation of knowledge. • Amass, analyze and/or trend key pharmacovigilance data to detect safety signals and prepare adequate responses to inquiries from regulatory authorities or challenges to product labels.
• Create and distribute high-quality reports that meet compliance requirements or fill the needs of internal customers for specialized data analysis. • Evaluate ADE data for accuracy and consistent entry and processing from source documents, with emphasis on compliance and quality.
• Initiate or participate in data mining activities to identify potential business opportunities.• Review publications to help maintain the literature database. Basic Qualifications DVM or equivalent.
• Fluently bilingual (English, French) written and verbal communication preferred.

About you

• Demonstrated veterinary practice and/or previous industry experience in Pharmacovigilance or Regulatory Affairs.
• Knowledge of PC package tools including word-processing (Word), spreadsheets (Excel) and presentations (PowerPoint). • Knowledge of documentation and business writing skills.
• Ability to effectively communicate verbally and in writing. • Ability to define problems, to collect data, to establish facts and draw valid conclusions.
• Ability to set priorities and manage multiple tasks independently and under pressure of timelines. • Ability to interpret a variety of technical instructions.
• Effective interpersonal and intercultural skills.

What we offer

Brunel Life Sciences provides global staffing, recruitment, and contracting solutions for Life Sciences, Pharmaceutical, Biotechnology and Healthcare organizations. Brunel Life Sciences plays a vital part of the Brunel International Group, with over 100 offices in 40 countries and approximately 13,000 employees around the globe.

About us

This role provides scientific expertise and professionalism in the collection, analysis, interpretation and/or communication of pharmacovigilance data, as a function of providing superior customer service, meeting regulatory requirements, and/or monitoring the status and risk/benefit profile of the company products.

Summary

  • Vacancy number: PUB117735
  • Location: Montreal
  • Market: Life Sciences & Health Care
  • hours per week: 24
  • Branche: Pharmaceutical
  • Education level: Professional Master
  • Area of Expertise: Safety
  • Closing date: Friday, June 1, 2018
Apply now

Feel free to contact

JS

Jeff Sondek

Account manager Brunel Canada Toronto

+1 416 244 2402 2161

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