Clinical Trials Disclosure Mgr

Amgen

Experience with clinical trial document redaction
Knowledge of eu ctr and clinicaltrials.gov disclosures
Ability to anonymize personal data and confidential information
Amgen harnesses biology and technology to fight the world's toughest diseases and deliver innovative medicines

Job Summary

  • Amgen harnesses biology and technology to fight the world's toughest diseases and deliver innovative medicines.
  • The role involves leading the preparation of clinical regulatory documents for public disclosure while ensuring compliance with US and EU regulations.
  • Candidates must manage projects, coordinate staff, and prioritize work to meet strict internal and external deadlines.

Matching Summary

Amgen harnesses biology and technology to fight the world's toughest diseases and deliver innovative medicines.

Skills & Requirements

Must-have

  • Experience with clinical trial document redaction
  • Knowledge of EU CTR and ClinicalTrials.gov disclosures
  • Ability to anonymize personal data and confidential information

Nice-to-have

  • Strong project management and prioritization skills
  • Excellent communication and cross-functional collaboration
  • Leadership experience in teaching and influencing teams

Key Requirements

  • Graduate degree plus 2 years pharmaceutical experience OR Bachelor's plus 4 years
  • Minimum 2 years experience preparing regulatory documents for public disclosure
  • Familiarity with international clinical transparency regulations and guidance

Work Rights

Not specified

Tailored Resume

Cover Letter