Bilingual Pharmacovigilance Associate

BioScript Solutions•Oakville, ON

1d•Remote

About The Position

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! 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?

Requirements

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
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 an asset
Comfortable working with computers and technology, specifically the Microsoft Office suite of products.
Bilingualism (French and English) is required for this position to effectively communicate with internal and external stakeholders.

Nice To Haves

Preference for an individual with CAPA investigation experience
Versed in Change Control Management is an asset

Responsibilities

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