(Senior) Regulatory Affairs Consultant CMC small molecules

Parexel
📍 Poland, Poland, Poland 💼 Full time 🕒 Posted March 01, 2026

Job Description

When our values align, there's no limit to what we can achieve.
 

Are you passionate about regulatory affairs in the life science industry? Do you thrive in a dynamic team environment and enjoy managing complex projects? Parexel is seeking a talented (Senior) Regulatory Affairs Consultant with CMC writing background (small molecule) to join our growing team!

As a (Senior) Regulatory Affairs Consultant CMC at Parexel, you will be at the forefront of managing and coordinating regulatory submissions across various markets. This role offers an excellent opportunity to develop your expertise in regulatory affairs while working with a diverse range of clients and stakeholders.

The role can be office or home based.

Role Responsibilities:

- Manage lifecycle maintenance activities, including renewals, variations, and responses to deficiency letters

- Coordinate submission and management work in Veeva Vault

- Collaborate...

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Job Details

  • Location Poland, Poland
  • Job Type Full time
  • Category Business Operations Specialists
  • Posted Date March 01, 2026
  • Application Deadline April 10, 2026