Regulatory Affairs Specialist for Pharmaceutical Compliance
hace 4 días
At ClinChoice, a global full-service CRO, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. This role is perfect for an individual who is passionate about ensuring pharmaceutical compliance and regulatory submissions.
Key Responsibilities:
We are looking for someone with excellent communication skills, attention to detail, and the ability to manage multiple tasks simultaneously. As a Regulatory Affairs Specialist, you will be responsible for reviewing new certificate requests, compiling NDA Annual Reports, and submitting them to the FDA. You will also be required to liaise with requesters, contractors, and consular services to ensure timely processing of requests.
Main Job Tasks and Responsibilities:
- Review new certificate requests and forward them to relevant suppliers for processing
- Compile NDA Annual Reports and submit them to the FDA
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