Bilingual Pharmacovigilance Associate – d’associé ou d’associée en pharmacovigilance

🕒 September 22

🇨🇦 Canada – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

💬 Bilingual

👻 Ghost score 18%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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BioScript Solutions

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2001

📦 Logistics

🏥 Healthcare

💊 Pharmaceuticals

Logistics • Healthcare • Pharmaceuticals

BioScript Solutions is a Canadian specialty pharmacy and specialty-care services provider that helps patients with chronic and complex conditions access specialty drug therapies. The company operates infusion clinics and pharmacies, runs patient support programs, and offers wholesale pharmaceutical distribution and third-party logistics to manufacturers, payors and healthcare practitioners across Canada. BioScript focuses on patient-centred care, medication delivery and care coordination to improve health outcomes and simplify access to specialty treatments.

📋 Description

• Manage collection, processing, and reporting of adverse events and reconciliation reports • Recognize, triage, and report adverse events according to program or manufacturer requirements • Maintain high compliance standards for reporting timelines and report quality • Respond to stakeholder inquiries • Conduct Pharmacovigilance compliance activities • Assist with investigations into late adverse-event reports • Perform work on rotating shifts of 8:00 a.m.–4:00 p.m. EST, 9:00 a.m.–5:00 p.m. EST, and 10:00 a.m.–6:00 p.m. EST • Work occasional weekends • Perform other tasks as required

🎯 Requirements

• BSc and/or BA related to Health Science • 1–3 years of experience in Pharmacovigilance, Medical Information, Adverse Event Reporting, Safety Case Processing, Regulatory, or QA • Good understanding of safety regulations • Experience in medical and/or pharmaceutical fields, including exposure to medical terminology and/or scientific writing is an asset • Exceptional organizational skills and strong attention to detail • Proven analytical and problem-solving skills • CAPA investigation experience preferred • Change Control Management experience is an asset • Proficient in conducting Program Compliance • Above-average verbal and written communication skills • Demonstrated prioritization skills and ability to multitask to meet tight deadlines • Bilingual English/French is required • Comfortable working with computers and technology, specifically Microsoft Office

🏖️ Benefits

• Flexible remote work options • Growth opportunities and career advancement support • Competitive salary • Incentive program • Comprehensive benefits package • Paid time for volunteering • Tree planted for each new hire • Accommodations available on request • Inclusive and accessible work environment

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