Source Job

US

  • Develops and directs global regulatory strategy to obtain and maintain product approvals across key regions.
  • Serves as primary regulatory contact for health authorities and leads cross-functional regulatory sub-teams.
  • Identifies regulatory risks and provides strategic guidance for product development and lifecycle management.

Regulatory Affairs Strategic Planning Cross-functional Leadership

3 jobs similar to Director, Global Regulatory Lead

Jobs ranked by similarity.

US

  • Serve as a regulatory representative on multidisciplinary program teams, supporting health authority interactions and global submissions for biologics in development.
  • Contribute to regulatory plans across the product lifecycle, from early clinical development through registration and lifecycle management.
  • Manage submission activities including INDs/CTAs, amendments, annual reports, and briefing documents, ensuring compliance with US/EU regulations and ICH guidelines.

Oruka Therapeutics (Nasdaq: ORKA) develops novel biologics to treat chronic skin diseases like plaque psoriasis, aiming for high rates of complete clearance with dosing as infrequently as once or twice per year. As a small startup building its core team, we seek top talent passionate about making a difference and contributing to an engaged, inclusive, and positive company culture.

US Unlimited PTO

  • Own the end-to-end lifecycle of FDA premarket applications, with an immediate focus on authoring and steering 510(k) submissions to clearance.
  • Operationalize and maintain compliance across diverse and intersecting jurisdictions, including FDA (Device, Drug & Compounding) and CMS (CLIA/CAP).
  • Build and scale the "Technical Playbook" for medical product operations, ensuring the company stays ahead of shifting state, federal, and international regulations.

Hims & Hers is a health and wellness platform committed to better health by offering affordable and personalized care. As a public company traded on the NYSE, they are normalizing health & wellness challenges and innovating on their solutions to make better health outcomes easier to achieve.

$217,000–$268,100/yr
US

  • Partner with Regulatory leads to manage regulatory filing subteams and subteam operations.
  • Develop and maintain high level and detailed regulatory timelines that utilize project management software tools.
  • Resolve submission execution issues by managing contingency plans with cross-functional stakeholder input and resolving delays or potential delays.

Ultragenyx is a biopharmaceutical company committed to addressing unmet medical needs in the field of rare diseases. With a focus on innovation and patient-centricity, they strive to develop life-changing treatments and improve the lives of patients and caregivers.