Roles & Responsibilities
• Develop, review, and manage clinical and regulatory documents
• Prepare study protocols, Clinical Study Reports (CSRs), and regulatory submissions
• Draft manuscripts and scientific publications
• Ensure compliance with ICH, GCP, and applicable regulatory guidelines
• Conduct literature reviews and support scientific communication
• Collaborate with clinical, regulatory, and scientific teams
• Maintain accuracy, clarity, consistency, and document quality
Qualifications
• Degree in Life Sciences, Pharmacy, Medicine, or related field
Experience
• Experience in medical writing or regulatory/scientific writing
Skills
• Strong knowledge of ICH, GCP, and global regulatory standards
• Excellent writing, editing, and analytical skills
• Attention to detail and document quality
• Ability to work in an on-site, collaborative environment
About the Organization
TrialGuna provides clinical research and regulatory support services, enabling high-quality scientific documentation and regulatory compliance across healthcare sectors.
Unlock refined AI insights.