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Role Description

Real Chemistry is looking for a Senior Manager, Insights & Evidence to join our growing team! The Senior Manager, Insights & Evidence supports evidence generation and synthesis that informs global value, access, and reimbursement strategy. This role will lead evidence-generation and evidence-synthesis workstreams to support value, access, and reimbursement strategy—translating complex clinical, economic, and real-world data into clear, decision-ready insights and narratives for internal teams and external stakeholders.

This is a hybrid role, based in any of our US offices—including Boston, Chicago, Carmel, Lambertville, or Wilmington—or remotely within the US, depending on team and business needs.

Key Responsibilities:

• Lead and execute evidence synthesis workstreams, including SLRs (protocol development, screening oversight, data extraction, and synthesis) and targeted literature reviews.
• Develop Global Value Dossiers (GVDs) and supporting modules (clinical, economic, humanistic, epidemiology/burden, unmet need), ensuring strong evidence traceability and version control.
• Support development of HTA submissions and payer evidence packages; contribute to JCA-aligned evidence planning and content.
• Translate evidence into strategic insights for market access and value strategy (e.g., value story, evidence gaps, evidence-generation recommendations).
• Ensure scientific rigor and editorial quality of deliverables (references, tables/figures, methodological transparency, compliance with client/style requirements).
• Manage project plans and junior staff/contractors (work allocation, feedback, quality review) to deliver on time and within scope.
• Stay current on evolving evidence standards and trends impacting access decisions, including:
  • HTA requirements and value frameworks
  • Payer evidence expectations and comparative effectiveness
  • RWE guidance and regulatory considerations
  • Measurement/reporting of quality, performance, and outcomes

Qualifications

• 6–9+ years of experience in HEOR, RWE, market access, medical writing, epidemiology, or related evidence-focused roles (consulting and/or biopharma experience preferred).
• Demonstrated hands-on experience with SLRs, GVD development, and HTA submission support; familiarity with JCA requirements and implications for evidence packages.
• Strong ability to synthesize and communicate complex evidence in clear, well-structured written deliverables (reports, dossiers, slide decks).
• Solid project management skills: scoping workstreams, managing timelines, coordinating reviewers, and maintaining high quality under deadline.
• Client-service orientation, sound judgment, high attention to detail, and ability to operate effectively in a fast-paced environment.
• Proficiency with Microsoft Office (PowerPoint, Excel, Word, Outlook).
• Bachelor’s degree required; advanced degree (MPH, PhD, PharmD, MD, MS) preferred in a relevant discipline.

Requirements

• Pay Range: $90,000-$100,000
• This is the pay range the Company believes it will pay for this position at the time of this posting. Consistent with applicable law, compensation will be determined based on job-related, non-discriminatory factors including but not limited to work experience, skills, certifications, and geographical location. The Company reserves the right to modify this pay range at any time.

Benefits

• Comprehensive benefit program and perks, tailored to your region.
• Free snacks in offices to keep you running all day long.
• Generous holiday and paid time off.
• Options for private medical, dental, and vision plans.
• Support in saving for the future.
• Mental wellness coaching and support.
• Access to more than 13,000 online classes with LinkedIn Learning.