Regulatory Affairs Consultant
Parexel(2 months ago)
About this role
Parexel is hiring a Consultant to support regulatory authority submissions for clinical trials, with a focus on Brazil and participation in global studies. The role operates within Parexel’s consulting frameworks and contributes to delivering regulatory submission work that aligns with client and internal quality expectations. The position may act as a Global or Regional Regulatory Lead for assigned studies.
Required Skills
- Regulatory Submissions
- Clinical Trials
- Brazilian Regulations
- Project Management
- Quality Control
- Regulatory Compliance
- DDCM
- DEEC
- Drug Development Plan
- Submission Management
+10 more
Qualifications
- Bachelor’s Degree (Scientific Or Technical Discipline)
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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