Duties and Responsibility

  • Independently write and QC/review patient narratives.
  • Maintain audit, SOP and training compliance.
  • Undertake project specific activities at high quality and in defined timelines according to standard processes and operating procedures
  • Master’s Degree in Science or Pharmacy.
  • Knowledge of global regulations and guidelines (FDA, ICH) that pertain to the drug development process.
  • Previous research or clinical experience in the pharmaceutical industry.
  • Experience and working understanding of electronic document management systems.
  • Relevant writing experience i.e. experience in narrative generation.
  • Clinical Study Report writing in therapeutic area, compound, the 4 phases of development and study designs.
  • Fluency in spoken and written English.
  • Good knowledge of basic computer applications including MS Word/PowerPoint/Excel.
Job Location: Gurgaon
Experience (Years): 2-5 Years

Apply for this position

Allowed Type(s): .pdf, .doc, .docx, .rtf