(Senior) Regulatory Affairs Consultant CMC small molecules
Parexel(3 months ago)
About this role
Parexel is hiring a (Senior) Regulatory Affairs Consultant focused on CMC writing for small-molecule products to support regulatory submissions across multiple markets. The position involves working with diverse clients and stakeholders while contributing to clinical development solutions that improve patient health. The role can be office-based or home-based, offering flexibility while supporting a growing regulatory affairs consulting team.
Required Skills
- Regulatory Submissions
- CMC Writing
- Module 1 Writing
- Module 3 Writing
- Lifecycle Management
- Renewals
- Variations
- Deficiency Responses
- Veeva Vault
- Project Leadership
+6 more
Qualifications
- University Degree In Life Science
About Parexel
parexel.comFor over 35 years Parexel has been a trusted global CRO and biopharmaceutical services company. Learn more about how we can help.
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