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Bilingual Pharmacovigilance Associate
Bilingual Pharmacovigilance AssociateBioScript Solutions • Oakville, ON, CA
Bilingual Pharmacovigilance Associate

Bilingual Pharmacovigilance Associate

BioScript Solutions • Oakville, ON, CA
Il y a plus de 30 jours
Type de contrat
  • Temps plein
  • Permanent
Description de poste

Empowering lives, healing hearts, embracing future 🌟

Insert Short description of role: Are you ready to make a lasting impact in specialty care? We’re seeking a dedicated and dynamic Bilingual 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.
  • 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.
  • Our People Say It Best:
  • Attractive Compensation: Competitive salary, incentive program, and comprehensive benefits package.
  • What & Where: Oakville, ON or Moncton, NB & Full-Time, Permanent
  • Closing Date: April 7, 2026

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;
  • Exceptional organizational skills and strong attention to detail;
  • Proven analytical and proven solving skills;
  • Preference for an individual with CAPA investigation experience;
  • Versed in Change Control Management is an asset;
  • Proficient in conducting Program Compliance;
  • Above average verbal and written communication skills;
  • Demonstrated prioritization skills and ability to multi-task to meet tight deadlines;
  • Bilingual, English/French is required;
  • Comfortable working with computers and technology, specifically the Microsoft Office suite of products.

Compensation: At BioScript, your base pay is one part of your total compensation package and is determined within a range. Our pay ranges are based on the local cost of labor benchmarks for each specific role, level, and geographic location.

We're proud to be an equal opportunity employer. As a people-centric organization, we’re committed to fostering a welcoming culture free of discrimination, and to providing a healthy and safe work environment where all team members can thrive as individuals. Through our commitment to diversity, inclusion, belonging, and equity, we strive to provide an accessible workplace, where individuals feel valued, respected, and supported every day.

We are committed to creating an inclusive and accessible work environment across Canada. In accordance with applicable provincial legislation, including Quebec’s Charter of the French Language, this job posting is provided in both French and English when required. For positions based in Quebec, French language proficiency is required to perform day-to-day duties. Bilingualism (French and English) is required for this position to effectively communicate with internal and external stakeholders.

We encourage and accept all applications, however, only candidates selected for interviews will be contacted. Accommodations can be made available on request for candidates taking part in all aspects of the selection process. For inquiries, please email the talent acquisition team at

Ready to make your mark? If you’re passionate about transforming ideas into extraordinary results and excited to join a forward-thinking team, we want to hear from you!

#INDA

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Bilingual Pharmacovigilance Associate • Oakville, ON, CA

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