Remote Bilingual Pharmacovigilance Associate
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Empowering lives, healing hearts, embracing future
Are you ready to make a lasting impact in specialty care? We’re seeking a dedicated and dynamic Pharmacovigilance Associate to join our Patient Support Programs at BioScript Solutions, where we put our patients first
What we offer (and why you’ll love it here):
- Epic Work-Life Balance: Flexible remote work options because we value your time and well-being. â¯
- Growth Opportunities: Committed to fostering a culture of growth, where every team, member is encouraged to pursue new skills, expand their knowledge, and advance their careers.
- Vibrant Culture: Over 1,500 team members across Canada and year over year we manage to maintain an overall above industry engagement score by using a monthly pulse survey.
- Attractive Compensation: Competitive salary, incentive program, and comprehensive benefits package.â¯â¯
- What & Where: Full Time, Permanent & Remote (Canada)
Why BioScript Solutions?
At BioScript, we're not just a company—we're a fast-growing company always putting patients first. Recognized as one of Canada’s Best Managed Companies, we believe in pushing boundaries, setting trends, and creating meaningful experiences that captivate and inspire. Our vibrant team is made up of innovative minds who are passionate about driving success and making an impact. Ready to be a part of this exhilarating journey?
Your Mission:
- Managing the collection, processing, and reporting of adverse events (AEs) and reconciliation reports
- Accountable for recognizing, triaging, and reporting as per the program or manufacturer
- requirements
- Maintaining high compliance standards regarding reporting timelines, quality of reporting, and
- responding to inquiries from stakeholders
- Help conduct Pharmacovigilance compliance activities
- Assisting in the initiation of investigations for late AE reports.
- Shift Rotation–8:00a.m.-4:00p.m. EST, 9:00a.m.-5:00p.m. EST, 10:00a.m.-6:00p.m EST. Occasional weekend work.
- Other tasks as required
What You Bring to the Table:
- BSc and/or BA related to Health Science;
- 1-3 years of experience in Pharmacovigilance/Medical Information/Adverse Event Reporting/Safety Case Processing experience and/or Regulatory or QA is an asset;
- Good understanding of safety regulations;
- Experience in medical and/or pharmaceutical field(s), including exposure to medical terminology and/or scientific writing is an asset;
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