Associate Director Access And Value - MEA

Who We Are

BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.

Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.

Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.

Summary Description

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The Associate Director, Access & Value MEA is responsible for driving, coordinating, and executing all delegated market access–related activities across the assigned countries.

The role ensures effective planning and implementation of market access strategies, health‑policy activities, payer engagements, early pipeline/new product planning, and cross‑functional collaboration to support BioMarin’s portfolio.

This position works in close alignment with the ICON Access & Value team, Medical Affairs, Marketing, legal and local Commercial teams to secure timely and sustainable access to BioMarin products for patients across diverse healthcare systems.

Success in this role requires a highly collaborative, transparent, and solution‑oriented working style to ensure smooth coordination across Commercial and cross‑functional teams.

Responsibilities

List the major responsibilities of the job.

• Create and maintain a Strategic Access Plan for all Biomarin products
• This position is responsible for all activities and execution of these Strategic Access Plan
• Design, prepare, and support relevant submissions to gain positive outcomes from Common Drug Review, public formularies as well as institutional buying groups.
• Identify, map and manage all KDM’s and their organizational relationships in key stakeholder groups (payer, government and physicians).
• To lead the all the activities for preparation of the Dossier (preparation, discussion, analysis, network with medical, Access and Commercial, legal ) and send to approval internally, in order to submit for different Government authorities
• Create and maintain relationships with each country KOL state´s REP´S.
• Recognize the process of accreditation the hospitals in SP.
• Prepare and send progress reports.
• Support the commercial area of each state. Country
• Support the commercial partners in the negotiations ,
  
  

SCOPE

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Middle east and African countries

EDUCATION

State both the minimum and the preferred educational attainment (or equivalent experience), and describe essential and desired subject matter, certifications, special training, etc.

• Bachelors degree or equivalent with a focus on Business or Sciences
• Fluent in English.
  
  

Experience

State both the minimum and the preferred number of years of relevant experience, and describe the essential functions of the job.

• Minimum 8+ years of experience working in strategy/operations.
• Strong experience in Public Relations, Public Affairs and Government relationships
• In-house experience at a pharmaceutical/biotechnology organization strongly preferred
• Excellent written, oral, communication, and presentation skills.
• Proven ability to work with all levels of management and commercial sales.
• Strong problem solving and organization skills.
• Knowledge and experience preparing and submitting dossiers and state formularies.
• Ability to review and analyze business and medical data.
• Ability to work competently in software programs including Word, Excel and Powerpoint
• Ability to work well in both a team environment and independently
• Demonstrated ability to collaborate effectively with others in addressing complex issues.
• Motivated, self-starter with ability to appropriately prioritize issues, allocate resources, and be capable of working alone and making sound decisions
• Customer-oriented thinking
• Demonstrate willingness to grow and develop with the company
  
  

Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.

Equal Opportunity Employer/Veterans/Disabled

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, or protected veteran status and will not be discriminated against on the basis of disability.

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