Hybrid Director, Regulatory Affairs – Precision Medicine, Digital Health

Posted 21 hours ago

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About the role

  • Lead regulatory strategy for precision medicine and digital health at GSK. Collaborate with teams to ensure compliant development across multiple regions including USA and UK.

Responsibilities

  • Lead development and execution of regional regulatory strategies for precision medicine and digital health assets
  • Coordinate regulatory interactions with local and regional health authorities and external partners
  • Provide regulatory input to cross-functional project teams from early development through lifecycle management
  • Ensure regulatory compliance for companion diagnostics, software as a medical device (SaMD), and digital health components
  • Interpret regulatory feedback and translate it into clear operational plans and submission materials
  • Mentor and coach colleagues to build regulatory capability across the business.

Requirements

  • Bachelor’s degree in biological science, healthcare science, engineering or equivalent
  • Experience working in the pharmaceutical industry, MedTech industry or regulating authorities
  • Practical experience with regulation of companion diagnostics and/or SaMD
  • Proven track record leading development, submission and approval activities in one or more regions
  • Experience preparing for and leading regulatory milestone meetings and authority interactions
  • Strong written and verbal communication skills and ability to work in a matrix environment.

Benefits

  • health care and other insurance benefits (for employee and family)
  • retirement benefits
  • paid holidays
  • vacation
  • paid caregiver/parental and medical leave
  • annual bonus
  • eligibility to participate in our share based long term incentive program

Job title

Director, Regulatory Affairs – Precision Medicine, Digital Health

Job type

Experience level

Lead

Salary

$171,750 - $286,250 per year

Degree requirement

Bachelor's Degree

Location requirements

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