Hybrid Associate STEM Content Analyst

Posted 2 months ago

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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

Job title

Associate STEM Content Analyst

Job type

Experience level

JuniorMid level

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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