Material Review Specialist

Biopharma Careers; Montreal (administrative region); Hybrid; CAD 70,000 - 95,000; Full time

Job summary

AbbVie Canada is seeking a Material Review Specialist in Montreal to lead medical/regulatory reviews for promotional and non-promotional materials. The role involves ensuring scientific accuracy, regulatory alignment, and collaboration with cross-functional teams.

You will also train internal stakeholders on review processes and regulatory expectations. Join AbbVie Canada to help maintain high standards of compliance, stay current with industry guidance, and contribute to metrics reporting for

Qualifications

• Experience reviewing promotional and non-promotional materials for medical/regulatory compliance.
• Knowledge of Canadian health product advertising regulations.
• Experience training internal stakeholders on review processes.
• Ability to generate metrics and reports on medical review activities.

Responsibilities

• Conduct high-quality medical/regulatory review of promotional and non-promotional materials and activities.
• Collaborate with internal stakeholders across functions.
• Provide training and guidance on medical review processes and applicable codes of practice.
• Support generation and presentation of metrics reports on medical review in designated therapeutic areas.

Skills

Medical review

Regulatory knowledge

Training & mentoring

Cross-functional collaboration

Regulatory codes & compliance

Job description

# Material Review SpecialistMontreal, QC Full-timeNotify me about similar jobsView Full Job & Apply at AbbVieAbbVie is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.## About this opportunityCompany Description**About AbbVie**AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.Job DescriptionJoining AbbVie means you will be part of a team of outstanding professionals dedicated to making a remarkable impact on patients' lives. At AbbVie, we conduct ground-breaking science on a global scale every day. AbbVie Canada is one of the Best Workplaces in Canada.When choosing your career path, choose to be remarkable.AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, vision care, virology, women’s health , and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio.We have a new opportunity for a Specialist, Material Review to join our Material Review team. In this role, the Specialist is responsible for the medical/regulatory review and approval of promotional and non-promotional materials.**Role:**Conduct a high-quality review of all promotional and non-promotional materials and activities according to internal SOPs, relevant Industry Codes and external laws and regulations. The incumbent will also provide training and advice to internal stakeholders on medical review processes, codes of practice and regulations.This role reports directly to the Manager, Material Review within the Medical Excellence/Medical Operations Department.**Key Responsibilities:**In assigned therapeutic area(s) (TA), perform the review of both Promotional and Non-Promotional Material on AbbVie’s products and their related disease states. Review the Material to ensure medical and scientific accuracy and adherence to applicable regulations, codes, and internal requirements.Collaborate closely with internal stakeholders.Stay current with knowledge of industry best practices, medical and regulatory requirements, Codes of Ethic/Practice, Preclearance Agencies.Provide guidance on project feasibility in consideration of Canadian regulations on health product advertising.Support the generation and presentation of metrics reports on medical review in designated TAs.