Regulatory Affairs Associate Director
GRAIL
Job Level
JuniorMid-Level
About the role
- Review/analyze and update the Pharmacological Activities and update the internal core database (CMS) according to guidelines.
- Review/analyze and update IN VITRO, IN VIVO and EX VIVO studies from patents, references, posters, press releases, and conferences in CMS.
- Record pharmacological parameters and units measured, materials and methods used in respective activities.
- Capture pharmacological details including animal model, dose regime, end point measurements and duration of drug.
- Achieve production volume and quality targets and record performance against targets.
- Take active role within team to ensure targets are met and maintain awareness of current developments.
- Maintain consistent quality standards, effective personal planning and time management, and adapt to process change.
- Identify training and development needs and promote personal and workplace safety.
- Undertake other reasonable duties as requested by line manager/director.
- Understand AI tools and techniques to enhance process efficiency and continuous improvement.
- Analyze journals, patents and meeting abstracts and provide pharmacological content to CDDI.
Requirements
- M Pharm, B. Pharm Graduates.
- 0 to 2 years experience in pharmacology content
- Knowledge in content analysis & editing
