IND RA (Senior) specialist
- 서울시
- 정규직
- 풀타임
- Prepare for clinical trial applications (IND or IND variation) according to the local and global strategy in collaboration with SM&M Korea.
- Implement/manage registration procedures required by Korean pharmaceutical regulations to achieve the earliest market entry.
- Harmonize Korean products labels and promptly notice to GRA about local impositions for the labelling from the MFDS to avoid any local issue. Update the safety information in line with the CDS and other reference countries.
- Product lifecycle maintenance: Keep product license to be compliant with regulations.
- Package compliance: Secure the package compliance in line with the local regulation and AZ compliance.
- Quality Control: Give advice to the QC lab based on regulatory knowledge and support the technical transfer.
- Responsible for company’s compliance into all relevant Korean and AZ’s procedure including Good Regulatory Practice (GRP).
- Review the compliance of promotional literatures from regulatory perspective.
- Maintain high level of authorities’ satisfaction through application of high professional standard in all contacts, quick resolution of authorities’ enquiries and provision of support.
- Maintain positive relationship with local contractors, customers and internal staff.
- Comply with the relevant regulations and AZK’s ethical business practices with full understanding of the code of conducts.
- Get any information relating to changes in the relevant regulatory regulations and health authorities and report to RA manager on any expected impact on our business.