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- Review, analyze, and update Pharmacological Activities in the internal core database (CMS) according to proposed guidelines.
- Review, analyze, and update IN VITRO, IN VIVO, and EX VIVO studies from patents, references, posters, and conferences in CMS.
- Document pharmacological parameters, units measured, materials, and methods used in respective activities from various sources.
- Detail pharmacological aspects of drugs including animal models, dosage regimes, endpoint measurements, and drug duration.
- Achieve production volume and quality targets.
- Record performance against targets.
- Actively participate in the team to ensure targets are met.
- Maintain awareness of current developments in relevant technology areas.
- Achieve and maintain consistent quality standards and practice effective personal planning and time management.
- Maintain a flexible and adaptable approach towards process changes.
- Identify technology training and developmental needs on an ongoing basis.
- Promote personal safety and that of others by adhering to safety practices and guidelines.
- Undertake any other reasonable duties as requested by the line manager/director on a permanent or temporary basis.
Product: Cortellis Drug Discovery Intelligence (CDDI) focuses on pharma and drug development, integrating essential biological, chemical, and pharmacological data from diverse sources into a single platform. It provides a comprehensive source of R&D intelligence curated and validated by scientists for scientists.
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