Market Access Consultant

Stratenym

4d

About The Position

The Market Access Consultant works on multiple complex pharmaceutical projects while maintaining quality, ownership, and accountability. The role requires thoughtful problem-solving, strategic recommendations, attention to detail, strong communication, and consistent delivery of high-quality work within project timelines. The Consultant leads projects from start to finish, interacts with clients, and may provide strategic guidance. Work includes researching, writing, and referencing product-specific pharmaceutical documents such as clinical summaries, reimbursement submissions, value stories and dossiers, manuscripts, conference abstracts and posters or presentations, and health-economic model technical reports. The Consultant manages time, timelines, and budgets, identifies out-of-scope requests, applies feedback, and contributes to business development where feasible. The position involves autonomous work and remote collaboration; occasional travel may be required. The expected starting salary is CAD $80,000, with transparent, performance-driven annual compensation adjustments and bonuses. Comprehensive health coverage includes medical, dental, and vision plans.

Requirements

• Advanced or professional degree (MSc, PhD, PharmD, or MD) in a scientific or medical discipline.
• Prior experience in the pharmaceutical or CRO industry, or at a medical communications agency.
• Demonstrated track record of success in a medical writing role, evidenced by factors such as years at an employer, promotions, or value of deliverables managed.
• Exceptional written and spoken English.
• Expert user of MS Word, PowerPoint, Excel, and reference management software such as EndNote.
• Familiarity with common biomedical terminology.
• Confident and professional demeanour, with comfort interacting with senior pharmaceutical company executives.
• Strong communication skills and exceptional attention to detail.

Nice To Haves

• Strong quantitative skills and a deep understanding of reporting statistical analyses of clinical-trial and epidemiologic data.
• Familiarity with principles and terminology of cost-effectiveness and budget-impact analyses.
• A portfolio or examples that are not bound by confidentiality.
• Knowledge of AMA style, GPP3, and ICMJE guidelines.

Responsibilities

• Research, write, and reference product-specific pharmaceutical documents, including clinical summaries, reimbursement submissions, value stories and dossiers, manuscripts, conference abstracts and posters or presentations, and health-economic model technical reports.
• Lead projects from start to finish, interact confidently with clients, and provide strategic guidance when needed.
• Manage time independently to meet deadlines and be available for web-based meetings during working hours.
• Work within planned project timelines and budgets, and identify out-of-scope requests in a timely manner.
• Implement corporate business development strategies to win new work where feasible, including recognizing client needs and advancing company products or services.
• Accurately and consistently implement editor, client, and management feedback.
• Work autonomously and collaborate remotely within a team environment.
• Travel occasionally, as required.

Benefits

• Annual compensation adjustments and bonuses that are fully transparent and performance-driven.
• Comprehensive health coverage, including medical, dental, and vision plans.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level