Added
36 minutes ago
Type
Full time
Salary
Salary not provided

Related skills

document management data interpretation clinical research medical writing pharmaceutical industry
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📋 Description

  • Serve as a primary author for routine medical and scientific documents, including clinical study
  • Support the development of more complex clinical, scientific, and programme-level documents, such
  • Review, interpret, and present complex clinical and scientific data accurately, concisely, and in a
  • Ensure assigned documents comply with applicable quality processes, standards, templates, and
  • Apply strong grammatical, editorial, proofreading, and scientific writing skills to produce clear
  • Support programme management activities, including contributing to timelines, budgets, forecasts

🎯 Requirements

  • Bachelor’s degree in a scientific discipline or an equivalent relevant academic or vocational
  • 3+ years of relevant professional experience demonstrating the knowledge and capabilities required
  • Experience within the pharmaceutical, biotechnology, clinical research, or CRO industry is
  • Previous experience in medical or scientific writing is advantageous, with strong grammar
  • Ability to understand, analyse, and communicate complex clinical or scientific data accurately and
  • Good understanding of regulatory documentation and the drug development process.

🎁 Benefits

  • Fully remote working opportunity from India.
  • Full-time position with a standard Monday–Friday schedule.
  • Opportunity to contribute to clinical research, drug development, and healthcare-related projects.
  • Collaborative environment focused on scientific excellence, innovation, and professional
  • Exposure to medical writing across clinical, scientific, and regulatory documentation.
  • Opportunities to work with internal teams and external clients across international projects.
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