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
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