Pharmacovigilance Coordinator
- ON, Canada
Full-time
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Job details
- Job type
- Full-time
- Apply by
- Experience
- Experience: 3+ years of experience in pharmacovigilance, patient/drug safety.
- Posting language
- English
- Posted
Original job description
Pharmacovigilance Coordinator (Contract ending October 2027) Remote - Ontario OR Quebec
Responsibilities
- 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.
- Cross-Functional Collaboration: Work closely with cross-functional teams, including regulatory, quality assurance, and medical affairs, to align on safety processes and requirements.
Requirements
- Bachelor's Degree in Science, or related field
- Experience: 3+ years of experience in pharmacovigilance, patient/drug safety.
- Language: French/English bilingual preferred.
- 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.
What We OfferWhy apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We'll get you going while you get on with the job.
About Us
Brunel has a reputation for working with some of the best in the business. That's what we continually strive for. Over 45 years, we've created a global network of interesting clients and talented individuals working together through a vast array of services.
More about this job
Responsibilities
The Pharmacovigilance Coordinator at Brunel will monitor, document and report adverse events under regulatory guidelines. They will keep pharmacovigilance data accurate and current, and work with regulatory, quality and medical affairs teams on safety processes.
Requirements
Brunel needs candidates with a science bachelor's degree and 3+ years of pharmacovigilance or patient or drug safety experience. Strong written and verbal communication, careful review of medical forms, independent work and comfort with safety and office software are required; French/English bilingualism is preferred.
Skills
- Adverse event monitoring and reporting
- Pharmacovigilance systems
- Data management
- Regulatory compliance
- Standard operating procedures
- Cross-functional collaboration
- Stakeholder communication
- Detail-oriented form review
- Independent work
- Office software
- Bilingual French and English
Categories
- Healthcare
- Science & Research
- Data & Analytics
Keywords
- pharmacovigilance
- drug safety
- patient safety
- adverse event reporting
- adverse events
- safety database
- case processing
- regulatory compliance
- standard operating procedures
- medical affairs
- quality assurance
- contract
- remote
- Ontario
- Quebec
- bilingual French English
- clinical safety
- pharmacy
Seniority
Mid level
Tools
- pharmacovigilance systems
- data management tools
- standard office software
Languages
- English
- French
Fields of study
- Science