Clinical Trials Regulatory Submission Sr. Associate

Amgen

Buenos Aires, Argentina
Regulatory submissions experience
Clinical trial project management
Strong communication skills
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 collaborative culture and supports professional growth and well-being.

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

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 regulatory submissions experience
  • Technical knowledge of ANMAT and CCIS

Work Rights

Not specified

Tailored Resume

Cover Letter