Scientific Writer

About Clinforge

Clinforge Clinical Research Solutions Pvt. Ltd. is a growing Contract Research Organization (CRO) dedicated to delivering high-quality services in 
clinical research, regulatory affairs, pharmacovigilance, and scientific/medical writing
. Our mission is to bridge science and communication by transforming complex research into impactful knowledge.

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.