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Lumanity

Healthcare value optimization and access facilitation

Senior Principal - Regulatory Strategy

Regulatory & Quality (Life Sciences)Posted on Nov 5
Full-timeUnited StatesRemote

About the Job

Requirements

  • Minimum 15 years of progressive regulatory experience in both consulting environments and in-house biopharma regulatory roles.
  • Direct experience leading regulatory strategies for development programs across multiple stages and therapeutic areas or product types.
  • Demonstrated success contributing to or managing regulatory workstreams, projects, and teams.
  • Ability to serve as a trusted advisor to pharmaceutical or biotechnology function heads and C-suite executives.
  • Expertise across pre-investigational new drug through post-market and access regulatory activities, including designations, accelerated approval pathways, and complex regulatory strategies.
  • Experience leading pre-investigational new drug meetings, Type C meetings, end-of-Phase 2 discussions, and other critical regulatory interactions.
  • International regulatory experience across major markets, including the European Medicines Agency, Health Canada, and the Pharmaceuticals and Medical Devices Agency, with working knowledge of global regulatory harmonization.
  • Deep regulatory expertise in at least one major therapeutic area, such as oncology, central nervous system, rare disease, or immunology, and working knowledge and comfort working across other therapeutic areas.
  • Experience across multiple product types, including small molecules, biologics, cell and gene therapies, and/or combination products.
  • PhD, Master of Public Health, or Master of Science in life sciences, regulatory affairs, or a related field.
  • Ability to generate business and meet individual sales or revenue targets, with experience managing engagement-level budgets.
  • Experience contributing to the development of new service offerings or capabilities within regulatory consulting.
  • Active engagement in regulatory thought leadership, speaking engagements, and/or recognition as a subject-matter expert within one's professional network.

Responsibilities

  • Advise pharmaceutical and biotechnology C-suite executives and function heads on regulatory matters that shape critical development, program-level, and portfolio-focused decisions.
  • Provide expert regulatory guidance on complex development programs, including novel modalities such as cell and gene therapy, biologics, and advanced therapeutics.
  • Collaborate with other practices to deliver integrated solutions addressing interconnected approval and access challenges.
  • Generate new business, meet individual sales targets through professional networks and the broader life sciences ecosystem, and secure new business with new clients.
  • Lead pursuit strategies for complex regulatory engagements and support practice business-development efforts, including mentoring junior consultants on business-development skills.
  • Develop multi-year account strategies for key relationships, identify priority client needs, shape demand across offerings, and secure repeat engagements.
  • Provide strategic oversight across engagements, proactively manage risk, protect delivery quality and client trust, ensure consistency and quality in regulatory strategy outputs, and balance profitability with client value.
  • Guide team members' development and mentorship, carrying direct reports when team structure and need require it.
  • Promote collaboration and knowledge sharing across markets and support reuse of regulatory frameworks and best practices.
  • Represent the company at industry forums and regulatory conferences to build external credibility and market presence.
  • Monitor the regulatory competitive landscape and share insights that inform practice positioning and service evolution.
  • Partner with the SVP to translate regulatory landscape changes, including artificial intelligence and digital submissions, global harmonization, and policy evolution, into practice growth opportunities.
  • Develop regulatory points of view and thought leadership that contribute to the company's positioning as an authoritative voice in regulatory strategy consulting.
  • Contribute to evolving consulting methodologies and developing new service offerings to address emerging regulatory challenges and client needs.

Desired Qualifications

  • MBA, Regulatory Affairs Professionals Society Regulatory Affairs Certification, or equivalent business/regulatory qualifications.

About the Company

Lumanity

Healthcare value optimization and access facilitation

Lumanity provides value-focused strategic consulting for life sciences brands to improve access to medicines. It builds data-backed plans that align scientific evidence with payer, provider, and patient needs and coordinates cross-functional teams to accelerate market access and evidence dissemination. Its approach emphasizes speed and flexibility with fresh perspectives tailored to each brand, focusing on how value is demonstrated and communicated to diverse stakeholders. Its goal is to unlock a brand's full potential by speeding access to therapies and ensuring stakeholders understand the medicines' value.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
New York City, New York
Founded
2022

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