Manager/associate Director, Therapeutic Group, Global Regulatory Affairs

GSK

Cambridge, MA, US
Base: $138,600 to $231,000; bonus/equity: annual b...
Hybrid (2-3 days on-site per week)
Regulatory affairs knowledge/experience
Develop regional regulatory strategies
Ensure execution of regulatory strategies
GSK is seeking a Manager/Associate Director for its Global Regulatory Affairs team, specifically within the Respiratory, Immunology & Inflammation therapeutic group. The ideal candidate will have experience in regulatory affairs, a strong understanding of drug development processes, and excellent interpersonal skills for cross-functional collaboration

Job Summary

  • As a valued member of the Regulatory Matrix Team and the asset project teams, you will be empowered to develop appropriate regional regulatory strategies and ensure their execution for assigned assets.
  • This role will provide YOU the opportunity to lead key activities to progress YOUR career.
  • The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role.

Matching Summary

Match Score: 85

GSK is seeking a Manager/Associate Director for its Global Regulatory Affairs team, specifically within the Respiratory, Immunology & Inflammation therapeutic group. The ideal candidate will have experience in regulatory affairs, a strong understanding of drug development processes, and excellent interpersonal skills for cross-functional collaboration.

Salary

Base: $138,600 to $231,000; Bonus/Equity: annual bonus and eligibility to participate in share based long term incentive program; Benefits: health care and other insurance benefits, retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave

Skills & Requirements

Must-have

  • Regulatory Affairs knowledge/experience
  • Develop regional regulatory strategies
  • Ensure execution of regulatory strategies
  • Lead regulatory interactions
  • Assess regulatory intelligence

Nice-to-have

  • Interpersonal skills
  • Good communicator
  • Strong listening skills
  • Foster collaborative working relationships
  • Work effectively within cross-functional teams

Key Requirements

  • Bachelor's degree in Biological Sciences, Healthcare Sciences, or related field
  • Experience in all phases of drug development in regulatory affairs
  • Advanced degree (e.g., PhD) preferred
  • Knowledge of clinical trials and licensing requirements
  • Proficient in digital tools and systems

Work Rights

Not specified

Tailored Resume

Cover Letter