Nordic Patient Access Director

15 hours ago


Stockholm, Stockholm, Sweden Sobi Full time

About the Role

We are seeking an experienced professional to lead our patient access efforts in the Nordic and Baltic regions. As Associate Director Patient Access Nordic Baltics, you will be responsible for developing and executing strategies that ensure timely and sustainable access to our therapies.

Your primary goal will be to build strong relationships with key stakeholders, including payers, health authorities, patient advocacy groups, and others. You will need to stay ahead of evolving health policy developments and analyze reimbursement trends to inform strategic decisions.

This is a single contributor role with no direct reports, but you will have the opportunity to work closely with cross-functional teams at both local and global levels.

About Sobi

Sobi is a specialized biopharmaceutical company dedicated to rare diseases. We focus on creating innovative treatments that make a positive impact on patients' lives. Our core values include Care, Ambition, Urgency, Ownership, and Partnership. We believe that our employees are our most valuable asset, and we strive to create a culture that supports growth and development.

What You Will Do

  • Develop and execute patient access strategies for Sobi products across the Nordic and Baltic regions
  • Become a subject matter expert on market access landscapes and reimbursement trends
  • Build and deepen relationships with key stakeholders to foster a supportive environment for patient access initiatives
  • Analyze data and develop insights to inform strategic decisions
  • Stay up-to-date on regulatory and reimbursement changes to adapt our strategies accordingly

Requirements

  • Masters degree in life sciences, health economics, or a related field
  • At least 5-10 years of experience working in pricing and patient access environments managing global brand pricing and strategy
  • Strong understanding of economic evaluation methods and study designs that produce clinically relevant data
  • Experience launching products in rare disease areas and navigating complex regulatory and reimbursement landscapes


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