Regulatory Affairs Specialist for Pharmaceutical Industry
3 hours ago
Salary: $90,000 - $120,000 per year
About the JobWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in Toronto, Ontario. As a key member of our regulatory team, you will be responsible for ensuring compliance with pharmacovigilance standards and regulations.
Key Responsibilities:- Cross-functional collaboration: Work closely with cross-functional teams, including regulatory, quality assurance, and medical affairs, to align on safety processes and requirements.
- Adverse event management: Monitor, document, and report adverse events in compliance with regulatory guidelines.
- Data management: Enter and maintain accurate data in pharmacovigilance systems, ensuring timely updates and reports.
- Communication: Serve as a liaison with internal and external stakeholders to address safety-related inquiries and provide updates.
- Compliance: Ensure adherence to all relevant regulations, guidelines, and standard operating procedures.
- Communication skills: Strong verbal and written communication skills, with the ability to collaborate effectively across teams.
- Attention to detail: Exceptional ability to review and process detailed medical and regulatory forms accurately.
- Independence: Self-starter with the ability to work independently and manage competing priorities.
- Tech savvy: Comfortable using pharmacovigilance systems, data management tools, and standard office software.
- Adaptability: Ability to hit the ground running and adapt to evolving workflows and timelines.
- Experience: Prior experience in pharmacovigilance, regulatory affairs, or related medical fields is an asset.
Brunel is a global recruitment agency with over 45 years of experience in matching talented individuals with top clients in various industries. We strive to provide exceptional service and support to our clients and candidates alike.
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