Global Value, Access and Commercialization Director
$196.4k - $245.5kSumitomo Pharma America, Inc.
Role Description
We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Global Value and Access Director – Regenerative Medicine. This individual will lead execution of market access, pricing, and reimbursement plans across global markets outside the US for regenerative medicine assets, while providing strategic input into the central global access strategy, value framework, and pricing guardrails. This role will partner with the Senior Director, Global Commercial and Market Access Strategy on OUS access strategy, evidence and value planning, cross-functional launch readiness, and early payer/access considerations across priority markets. This individual will work with the global cross-functional team and external partners to ensure that access, reimbursement, and value considerations are embedded early and operationalized effectively.
The ideal candidate brings strong strategic market access experience, excellent cross-functional leadership skills, and the ability to translate complex clinical and operational realities into actionable value and reimbursement strategies in highly specialized or innovative therapeutic areas.
Job Duties and Responsibilities
- Lead OUS Market Access Strategy and plan and an overall commercialization Execution
- Lead development and execution of OUS market access, pricing, and reimbursement strategies across priority OUS markets, aligned with centrally defined global strategy
- Translate overall global strategic objectives into actionable OUS launch plan including the market access workstreams, milestones, and deliverables aligned with global timelines
- Own and drive day-to-day execution of OUS market access priorities across assets, ensuring alignment to central strategy, timelines, and long-range plans.
- Drive OUS launch readiness activities related to access pathways, reimbursement planning, and pricing implementation
- Identify market-specific access risks, reimbursement barriers, policy constraints, and operational dependencies that may impact OUS launch readiness or uptake
- Contribute to long-range planning for international access, including launch sequencing assumptions, affordability considerations, and stakeholder engagement priorities
- Provide structured ex-US market insights to inform global access strategy, evidence planning, and value narrative development
- Lead HTA planning and execution across priority markets, including EU JCA and relevant country-level reimbursement pathways
- Develop country-level pricing and reimbursement recommendations aligned with centrally defined pricing guardrails
- Support pricing and reimbursement negotiations in partnership with regional stakeholders, affiliates, and external partners as applicable
- Monitor international pricing, reimbursement, and policy developments—including reference pricing and analogous cross-market risks—and recommend mitigation strategies
- Represent ex-US access perspectives in cross-functional planning and governance forums, escalating key tradeoffs and recommendations as appropriate
- Accountable for OUS access outcomes, including HTA success, reimbursement readiness, pricing alignment, and time to market access
Qualifications
- Bachelor’s degree required; advanced degree preferred (e.g., MBA, MPH, PharmD, PhD, MS, or equivalent)
- 10+ years of progressive business experience in the healthcare, pharma or biotech industry, inclusive of global market access, pricing & reimbursement, value strategy, HEOR interface, or global commercial strategy; experience in cell, gene, and regenerative medicines a plus
- Experience with EU markets and country-level HTAs, pricing and reimbursement; JCA experience preferred
- Strong understanding of payer, reimbursement, HTA, and access dynamics in OUS settings
- Ability to synthesize clinical, economic, operational, and policy information into clear strategic recommendations
- Excellent communication, executive presence, and stakeholder management skills
- Experience in rare disease, specialty therapeutics, biologics, cell therapy, gene therapy, tissue-based therapies, or other advanced modalities highly preferred
- Experience partnering with regional teams, affiliates, distributors, or external commercialization partners
- Comfort operating in a dynamic, ambiguous environment where access strategy must be developed in parallel with evolving clinical and regulatory plans
- Must be comfortable spending 30% of time traveling; some overnight travel required
Requirements
- The base salary range for this role is $196,400.00 - $245,500.00
- Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state.
- Our robust time-off policy includes flexible paid time off, 11 paid holidays plus additional time off for a shut-down period during the last week of December, 80 hours of paid sick time upon hire and each year thereafter.
- Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education and other factors permitted by law.
Benefits
- Merit-based salary increases
- Short incentive plan participation
- Eligibility for our 401(k) plan
- Medical, dental, vision, life and disability insurances
- Flexible paid time off
- 11 paid holidays plus additional time off for a shut-down period during the last week of December
- 80 hours of paid sick time upon hire and each year thereafter
$240k - $265k
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