Scientific Writer

About Clinforge

clinical research, regulatory affairs, pharmacovigilance, and scientific/medical writing

Key Responsibilities

• Develop, write, and edit 

  scientific manuscripts, review articles, case studies, and conference abstracts/posters

  .
• Prepare 

  regulatory and clinical documents

   (clinical study reports, investigator brochures, patient information leaflets, regulatory dossiers).
• Create 

  medical communication materials

   including slide decks, CME content, and white papers for healthcare professionals.
• Collaborate with researchers, clinicians, and regulatory teams to ensure 

  accuracy, consistency, and compliance

  with journal/regulatory requirements.
• Conduct 

  literature reviews

   and ensure referencing accuracy (PubMed, Scopus, etc.).
• Ensure documents follow 

  ICMJE, GCP, CONSORT, and journal-specific guidelines

  .
• Maintain high standards of 

  clarity, accuracy, and scientific integrity

  .

Qualifications & Skills

• Master’s or PhD in 

  Life Sciences / Pharmacy / Biotechnology / Clinical Research

  .
• 1–3 years of experience in 

  scientific or medical writing

   (Fresher with strong writing skills may be considered).
• Strong command of 

  English language, grammar, and scientific terminology

  .
• Familiarity with 

  journal submission processes

   and reference management software (EndNote, Mendeley, Zotero).
• Knowledge of 

  regulatory writing

   (CSR, CTD/eCTD modules) will be an added advantage.
• Excellent communication, attention to detail, and ability to meet deadlines.