TrialGuna, a growing organization in clinical research and regulatory services, is inviting applications for the position of Medical Writer / Regulatory and Scientific Writing Associate in Bengaluru, Karnataka. This is a full-time, on-site opportunity for professionals with regulatory medical writing experience who can develop, review, and manage high-quality clinical and regulatory documents in compliance with global guidelines.

This role is ideal for candidates seeking a career in regulatory medical writing, scientific writing, and clinical documentation across pharmaceuticals, medical devices, nutraceuticals, and related healthcare domains.

🧾 Key Responsibilities

• Develop, review, and manage clinical and regulatory documents including:
  • Study protocols
  • Clinical Study Reports (CSRs)
  • Regulatory submissions
  • Manuscripts and scientific publications
• Ensure compliance with ICH, GCP, and other applicable regulatory guidelines
• Collaborate with cross-functional teams (clinical, regulatory, and scientific affairs)
• Conduct literature reviews and support scientific communication
• Maintain accuracy, clarity, consistency, and quality across deliverables

🎓 Qualifications & Skills

• Degree in Life Sciences, Pharmacy, Medicine, or related field
• Experience in medical writing / regulatory scientific writing
• Knowledge of ICH, GCP, and global regulatory standards
• Strong writing, editing, and analytical skills
• Ability to work in an on-site, collaborative environment

💼 Benefits

• Full-time employment with TrialGuna
• Exposure to regulatory and clinical documentation projects
• Opportunity to work with experienced scientific and regulatory professionals
• Career growth in medical and regulatory writing

📍 Job Location

Bengaluru, Karnataka, India (On-site)

📩 How to Apply

Application Link