Bilingual Pharmacovigilance Associate

BioScript Solutions; City of Moncton; On-site; CAD 60,000 - 80,000; Full time

Job summary

A healthcare solutions company is seeking a Pharmacovigilance Associate to manage reporting and compliance functions related to adverse reactions. The role requires strong analytical skills, attention to detail, and fluency in English and French. This full-time position is based in Moncton, NB, with a focus on quality assurance and compliance activities.

Benefits

Environmental sustainability initiative

Qualifications

• 1-3 years of experience in Pharmacovigilance or related fields.
• Good understanding of safety regulations.
• Experience with medical terminology and scientific writing.
• Proficient in conducting Program Compliance.

Responsibilities

• Manage the collection, processing, and reporting of adverse events.
• Maintain compliance regarding reporting timelines and quality.
• Conduct Pharmacovigilance compliance activities.
• Assist in investigations for late adverse event reports.

Skills

Attention to detail

Analytical skills

Bilingual (English/French)

Organizational skills

Problem-solving

Education

BSc or BA related to Health Science

Tools

Microsoft Office

Job description

Overview

Your future starts here

We are looking for a meticulous individual with attention to detail to assume the position of Pharmacovigilance Associate (PV). The key functions include managing the collection, processing and reporting of Adverse Reactions (ARs) and Product Quality Complaints (PQPs) in accordance with corporate and national pharmacovigilance requirements. In addition to these core functions, the ideal candidate would also assist with quality assurance related tasks such as audit preparation, CAPA investigations, change management and program compliance.

Responsibilities

• Managing the collection, processing, and reporting of adverse events (AEs) and reconciliation reports
• Maintaining high compliance standards regarding reporting timelines, quality of reporting, and responding to inquiries from stakeholders
• Accountable for recognizing, triaging, and reporting as per the program or manufacturer requirements
• Help conduct Pharmacovigilance compliance activities
• Assisting in the initiation of investigations for late AE reports
• Shift Rotation – 8:00 a.m.–4:00 p.m., 9:00 a.m.–5:00 p.m., 10:00 a.m.–6:00 p.m.; occasional weekend work
• Other tasks as required

Qualifications

• BSc and / or BA related to Health Science
• 1-3 years of experience in Pharmacovigilance / Medical Information / Adverse Event Reporting / Safety Case Processing, and / or Regulatory or QA experience is an asset
• 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
• 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 a requirement
• Comfortable working with computers and technology, specifically the Microsoft Office suite of products

Benefits

With one tree planted for every new hire, why not start your new job on a green foot and help us lower our carbon footprint.

Job Status : Full Time, Permanent

Job Location : Oakville, ON or Moncton, NB

Application Deadline : October 1st, 2025