Clinical Trials Regulatory Submission Sr. Associate

Amgen UK

Buenos Aires, Argentina
Regulatory submissions experience
Clinical trial project management
Strong communication skills in english
Amgen is dedicated to serving patients living with serious illnesses through innovative medicines

Job Summary

  • Amgen is dedicated to serving patients living with serious illnesses through innovative medicines.
  • The role involves performing regulatory submissions and managing clinical trial projects in Argentina.
  • Amgen offers a competitive benefits package and supports professional growth.

Matching Summary

Amgen is dedicated to serving patients living with serious illnesses through innovative medicines.

Skills & Requirements

Must-have

  • Regulatory submissions experience
  • Clinical trial project management
  • Strong communication skills in English

Nice-to-have

  • Experience with Import License extensions
  • Ability to manage multiple projects
  • Collaborative team environment

Key Requirements

  • Master’s degree or Bachelor’s with 5 years experience
  • Minimum 3 years of regulatory submissions experience

Work Rights

Not specified

Tailored Resume

Cover Letter