Global Clinical Trial Submission And Portfolio Senior Manager

Pfizer

Poland
Base: 249,750 pln; bonus: 20%; benefits: compyny c...
Fully remote
6+ years regulatory affairs experience
Drug development knowledge
Submission management expertise
The role involves directing the development, quality control, and publication of submissions relating to asset development and registration while ensuring adherence to global regulations

Job Summary

  • The role involves directing the development, quality control, and publication of submissions relating to asset development and registration while ensuring adherence to global regulations.
  • Candidates will lead complex division-wide projects, drive strategic plans, and serve as a regulatory operational liaison throughout the product lifecycle.
  • The position offers a remote work arrangement with a minimal annual gross base salary of 249,750 PLN, a 20% bonus, and benefits including a company car and comprehensive health insurance.

Matching Summary

The role involves directing the development, quality control, and publication of submissions relating to asset development and registration while ensuring adherence to global regulations.

Salary

Base: 249,750 PLN; Bonus: 20%; Benefits: Company car, Medicover, UNIQA, Multisport, PPE

Skills & Requirements

Must-have

  • 6+ years regulatory affairs experience
  • Drug development knowledge
  • Submission management expertise
  • Microsoft Office Suite proficiency
  • Strategic planning capabilities

Nice-to-have

  • AI tool usage experience
  • Statistical modeling skills
  • Generative technology familiarity
  • Emerging markets collaboration
  • Process innovation mindset

Key Requirements

  • BA/BS degree with 6+ years experience
  • MBA/MS with 5+ years experience
  • PhD/JD with 1+ years experience
  • MD/DVM with 0+ years experience
  • Advanced Microsoft Office skills

Work Rights

Not specified

Tailored Resume

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