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)
Bachelor's degree in biological sciences
Experience in all phases of drug development
Regulatory affairs knowledge and experience
GSK is seeking a Manager/Associate Director for its Global Regulatory Affairs team, focusing on Respiratory, Immunology, and Inflammation. The ideal candidate will have experience in regulatory affairs and drug development, with strong interpersonal skills to lead regional regulatory strategies

Job Summary

  • The role involves proactively developing regulatory strategies that deliver the needs of local regions while aligning with global Medicines Development Strategy.
  • Candidates will lead regulatory interactions and review processes in their local region while ensuring compliance with all global and regional requirements.
  • This position offers a hybrid work arrangement requiring two to three days on-site per week along with eligibility for an annual bonus and share-based long-term incentive program.

Matching Summary

Match Score: 85

GSK is seeking a Manager/Associate Director for its Global Regulatory Affairs team, focusing on Respiratory, Immunology, and Inflammation. The ideal candidate will have experience in regulatory affairs and drug development, with strong interpersonal skills to lead regional regulatory strategies.

Salary

Base: $138,600 to $231,000; Bonus/Equity: Annual bonus and share-based long term incentive program; Benefits: Health care, retirement, paid holidays, vacation, and parental leave

Skills & Requirements

Must-have

  • Bachelor's degree in Biological Sciences
  • Experience in all phases of drug development
  • Regulatory affairs knowledge and experience

Nice-to-have

  • Advanced degree such as PhD preferred
  • Strong communication and listening skills
  • Ability to foster collaborative relationships

Key Requirements

  • Bachelor's degree required
  • Experience in all phases of drug development
  • Knowledge of clinical trials and licensing requirements

Work Rights

Not specified

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