Market Access & Value Evidence Lead- REMOTE
Engagement: Contingent contract, approximately 10–15 hours per week
Schedule: U.S. East Coast business hours
Anticipated term: Late 2026 through 2027, with potential extension based on business needs
About the Role
We’re seeking an experienced Market Access & Value Evidence Lead to bring market access and evidence perspectives to early-stage microbiome development programs. As an embedded member of cross-functional asset teams, you’ll help identify the payer, reimbursement, pricing, patient-population, and evidence questions that should inform development strategy.
The role will support programs across oncology and gastrointestinal (GI) areas, with a primary focus on the U.S. market and consideration of relevant European requirements. You’ll contribute to program discussions and help teams address future access considerations early—when they can still shape target product profiles and clinical development plans.
This is a part-time, strategic role suited to an independent professional who can exercise sound judgment with evolving information, influence cross-functional decisions, and translate clinical and scientific developments into practical recommendations.
What You’ll Do

• Represent market access and value evidence perspectives on assigned asset teams.
  

• Contribute to target product profiles, endpoint strategy, evidence plans, and development decisions.
  

• Assess potential pricing, reimbursement, and access implications of development options.
  

• Identify evidence and stakeholder questions early enough to inform program strategy.
  

• Translate clinical and scientific information into clear, actionable recommendations.
  

• Support research involving payers, distributors, pharmacies, and other relevant stakeholders.
  

• Prepare research briefs and scopes of work for targeted external engagements.
  

• Manage vendors and research partners for commissioned activities.
  

• Synthesize research findings and monitor relevant developments in pricing, access, evidence, and policy.

What You’ll Bring
Required

• Experience in market access, value evidence, pricing, reimbursement, payer strategy, HEOR, or a related biopharmaceutical function.
  

• Experience contributing to cross-functional development or asset teams.
  

• Experience supporting development-stage programs.
  

• Experience managing external vendors or research partners.
  

• Strong analytical, communication, and problem-solving skills.

Preferred

• Understanding of how development decisions can shape future market access and commercial success.
  

• Ability to quickly learn new topics and turn them into useful recommendations.
  

• U.S. market access expertise, with the ability to consider relevant European requirements.

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