Pharmacovigilance Associate

Sentrex; Markham; Hybrid; CAD 60,000 - 73,000; Full time

Benefits offered by this job

Competitive salary

Vacation entitlement

Wellness Program

Paid Sick Days

Benefits package including health

RRSP Matching

Employee Assistance Program

Job summary

Sentrex Health Solutions in Markham, ON is seeking a Pharmacovigilance Associate. This full-time role combines hands-on AE processing with QMS administration in a hybrid work environment requiring 2–3 days in the office weekly.

You will manage adverse event collection and reporting, ensure compliance with Health Canada GVP, and collaborate with internal teams to improve processes. The position offers a competitive salary and benefits, with strong growth opportunities within a Canadian company.

Qualifications

• 3+ years of Pharmacovigilance experience.
• Experience in Pharma with Health Canada GxP regulations.
• Proficient with Microsoft Office and databases.
• Strong organizational skills and attention to detail.
• Bilingual English/French is an asset.

Responsibilities

• Manage collection, processing, and reporting of adverse events (AEs).
• Ensure compliance with pharmacovigilance requirements across the organization.
• Maintain PV information and audit readiness for manufacturers and programs.
• Maintain high quality reporting timelines and respond to stakeholder queries.
• Record and report AE data per program or manufacturer rules.
• Submit reportable AEs to manufacturers per Health Canada guidelines.
• File and archive PV documents for audit readiness.
• Create/review SOPs and WIs as needed.
• Conduct PV trainings as needed.
• Coordinate with internal teams to improve processes.
• Assist with administering the QMS.

Skills

Pharmacovigilance

Microsoft Office

Communication skills

Teamwork

Tools

QMS

Job description

Job Category: Quality and Pharmacovigilance

Requisition Number: PHARM003223

• Posted : October 9, 2026
• Full-Time
• Hybrid

Locations

Showing 1 location

Description

Position Type: Full Time

Department: QA & PV

Work Location: Markham, ON

Work Arrangement: Hybrid - (in office 2-3 days a week will be required)

Work Hours: Standard Business Hours Monday to Friday

Travel Required: No

A proudly Canadian company, Sentrex Health Solutions is a fully integrated specialty distributor and patient support provider for pharmaceutical manufacturers, physicians, and their patients. We provide innovative solutions focused on ensuring patients have access and the support they need to maximize their treatment outcomes. We do this through strategic distribution models and patient support programs that are backed by powerful, integrated technology, a dedicated in-house creative agency, and experienced, cross-functional teams. Our core capabilities includeSpecialty Pharmacy Services, Customized Solutions for Warehouse, Wholesale & Distribution, Patient Support Programs, Strategic Creative Services as well as HCP & Clinic Services.

Come and join our team! But first, let us tell you why we love working here:

• We are 100% Canadian with locations across the country
• State-of-the-art facilities to provide high-quality products and services
• The opportunity to be a part of a winning, high-performing team
• Collaborative, engaging workplace culture – we are passionate about our people!
• Flexible working environment that promotes a healthy work-life balance
• Diverse and inclusive culture where your talent and commitment to excellence is welcomed and valued
• High-growth environment that provides opportunities for learning and growth supported by our Employee Development Program and industry-leading, in-house corporate training offered throughout the year
• Quarterly virtual social events!

The Opportunity:

The Pharmacovigilance (PV) Associate is a role based in our facility in Markham and the key functions include managing the collection, processing, and reporting of Adverse Events (AEs) and Product Complaints in compliance with all organization and national pharmacovigilance requirements. The PV Associate will also be responsible for helping out with administrative aspects of the Quality Management System (QMS) to help drive compliance with GxP regulations through the QMS

A Day in the Life (What you will do here):

• Managing the collection, processing, and reporting of adverse events (AEs);
• Adhering and contributing to the structure and objective of compliance across the organization.
• The organization, accuracy, and completeness of pharmacovigilance information for a variety of manufacturers and patient assistance programs, including audit preparation and management of Pharmacovigilance inbox
• Maintaining high compliance standards in regard to reporting timelines, quality of reporting, and assisting with responding to and tracking queries from stakeholders and manufacturers.
• Collecting, and recording data related to AE cases. Accountable for recognizing, triaging, and reporting as per the program or manufacturer requirements.
• Reporting and submitting reportable AEs to manufacturers as per Health Canada regulations and client guidelines.
• Electronic filing and archiving of PV documents to maintain audit readiness at all times
• Creating and reviewing Standard Operating Procedures (SOPs) and Work Instructions (WIs) as needed
• Conduct Pharmacovigilance trainings as needed
• Conducts period case reconciliation with applicable departments and clients as needed
• Collaborate with the internal SHS teams to help to find process efficiencies
• Help with administrating the Quality Management Systems
• Other tasks as required

What you need to ensure you are set up for success:

Bilingualism (English and French) is an asset

3+ years of experience in Pharmacovigilance or relevant industry experience

3+ years of experience in the Pharma environment that is familiar with Health Canada rules and regulations relating to GxP processes.

Good understanding of Health Canada GVP regulations

Proficient in the Microsoft Suite of products with the ability to work in various databases

Exceptional organizational skills and strong attention to detail.

Demonstrated prioritization skills and ability to multi-task to meet tight deadlines.

Proven analytical and problem-solving skills.

Above average verbal and written communication skills.

Ability to work as part of a team and have a collaborative mind-set to work with cross-functional partners;

Experience with QMS is an asset.

What makes you a great fit for this team:

• Your commitment to providing a high level of service to your internal and external clients.
• You are highly adaptable with a track record of success during times of growth and organizational change.
• You have a proven track record of developing trust and influence at multiple levels.
• You demonstrate an impactful and candid communication style.
• You have exceptional organizational skills with the ability to build effective working relationships with colleagues, management, and stakeholders.

We value our employees! Our permanent full-time employees are provided with a:

• Competitive Salary and generous vacation entitlement
• Wellness Program (5 paid days off for your well-being!)
• Paid Sick Days
• Competitive Benefits Package including Dental & Extended Health Benefits, AD&D, LTD & Employee/Dependent Life Insurance
• Employee & Family Assistance Program
• RRSP Matching Program
• The anticipated base salary hiring range for this role is $60k to $73k annually. The final base salary will be determined based on relevant experience, skills, and internal equity.

Sentrex Health Solutions is proud to be an equal opportunity employer demonstrated by our commitment to diversity, inclusion, belonging, equity, and accessibility. We provide a safe space for all team members to express their individuality within our corporate culture.

Accommodations can be made available upon request for those candidates taking part in the selection process.

Sentrex hiring managers may use artificial intelligence tools to assist them in the recruitment process.