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About the Role

IQVIA's Price Regulation Consulting team provides strategic, scientific, and regulatory consulting services to pharmaceutical companies operating within Canada's evolving pharmaceutical pricing environment. The team supports the full spectrum of PMPRB-related needs, helping clients create a Canadian pricing strategy for patented medicines considering international prices, launch sequence, and scientific evidence within the new regulatory framework.

Responsibilities

Conduct and lead reviews of clinical trial publications, treatment guidelines, product monographs, health technology assessments, and other scientific literature.
Assess and synthesize clinical evidence and pricing information relevant to therapeutic comparisons, price assessments, and regulatory submissions.
Summarize disease areas, standards of care, treatment pathways, unmet medical needs, and pricing context in a clear and objective manner.
Understand complex treatment regimens and evaluate how regimen differences, dose intensity, package configuration, and treatment duration may affect price comparisons.
Analyze Canadian and international price data for therapeutic class comparators to support evidence-based client recommendations.
Develop scientifically rigorous reports, pricing assessments, presentations, and client-submissions with conclusions supported by evidence and documented project requirements.
Manage client workstreams and lead day-to-day project execution.
Communicate regularly with clients to clarify objectives, discuss findings, and address project-related questions.
Design, structure, and deliver presentations tailored to technical and executive audiences.
Develop evidence-based recommendations that address client needs and support strategic decision-making.
Lead the preparation of PMPRB-related submissions, regulatory correspondence, and other client deliverables.
Manage multiple concurrent projects with competing timelines and priorities.
Develop project plans, monitor timelines, coordinate resources, and identify risks proactively.
Ensure deliverables meet quality standards, budget expectations, and client requirements.
Contribute to continuous improvement initiatives, including development of templates, processes, and knowledge resources.
Provide guidance and coaching to Consultants and Data Coordinators.
Review project work for accuracy, completeness, and scientific rigor.
Share subject matter expertise and contribute to the development of team capabilities.
Support onboarding and training of new team members.

Requirements

Master's degree, PharmD, PhD, or equivalent advanced training in Life Sciences, Pharmacy, Epidemiology, Public Health, Health Sciences, or a related discipline.
4–7 years of experience in pharmaceutical consulting, market access, regulatory affairs, medical affairs, health technology assessment, or a related healthcare environment.
Demonstrated experience conducting and interpreting scientific literature reviews.
Strong understanding of clinical trial design and interpretation of scientific evidence.
Excellent written communication skills, including preparation of scientific reports and client-facing documents.
Strong verbal communication and presentation skills.
Proven ability to manage multiple projects and consistently deliver against deadlines.
Advanced proficiency with Microsoft Word, Excel, and PowerPoint.
Strong analytical, organizational, and critical thinking skills.

Skills

Scientific Review & Pricing Analysis
Client Delivery
Project Management
Team Development
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Analytical skills
Organizational skills
Critical thinking skills
Written communication skills
Verbal communication skills
Presentation skills
Scientific literature reviews
Clinical trial design interpretation
Pharmaceutical pricing
PMPRB-related consulting
Canadian reimbursement processes
Market access processes
Systematic literature reviews
Evidence synthesis
Health technology assessment
Power BI

Experience Level

Senior Consultant
4-7 years of experience

Education Level

Master's degree
PharmD
PhD
Equivalent advanced training in Life Sciences, Pharmacy, Epidemiology, Public Health, Health Sciences, or a related discipline

Salary/Compensations

$114,000.00 - $152,000.00

Benefits

Health benefits
Wellness benefits
Other benefits

About the Company

IQVIA is the world leader in the provision of health and pharmaceutical insights to the health care sector.
IQVIA's Price Regulation Consulting team provides strategic, scientific, and regulatory consulting services to pharmaceutical companies operating within Canada's evolving pharmaceutical pricing environment.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Equal Opportunity

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law.
Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request.
IQVIA is committed to integrity in its hiring process and maintains a zero tolerance policy for candidate fraud.
All information and credentials submitted in your application must be truthful and complete.
Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
We may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making.