Regulatory Affairs Consultant
Parexel(13 days ago)
About this role
Parexel is seeking a Regulatory Affairs Consultant to prepare clinical and regulatory documentation for trials and provide consulting services to ensure regulatory compliance. The role involves authoring submissions, interpreting regulatory data, and advising on drug development pathways. It offers flexibility to work remotely within the United States.
Required Skills
- Regulatory Submissions
- FDA Regulations
- Project Management
- Drug Development
- Clinical Trials
- Regulatory Affairs
- INDs
- MRLs
- Fast Track Applications
- Orphan Drug Applications
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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