Job Responsibilities:
- Prepare, write, review, and edit medical, scientific, and regulatory documents including study protocols, informed consent forms (ICFs), clinical study reports (CSRs), summaries, manuscripts, and presentations
- Conduct comprehensive literature searches and synthesize scientific data into clear, concise, and accurate content
- Ensure compliance with ICH-GCP, regulatory guidelines, ethical standards, and internal SOPs
- Maintain version control and proper document management as per Quality Management System (QMS) requirements
- Collaborate with cross-functional teams (clinical, biostatistics, regulatory, and QA) to support documentation needs
- Respond to internal and external review comments and revise documents accordingly
- Support preparation of submission-ready documents and publications
- Ensure accuracy, consistency, and timely delivery of assigned documents
Qualifications & Experience:
- BDS / BAMS / Pharm D
- Minimum 2+ year of experience in medical or scientific writing
- Knowledge of clinical research terminology, ICH-GCP, and regulatory documentation
- Experience in clinical research, CRO, pharmaceutical, or healthcare environments preferred
Core Competencies:
- Excellent written and verbal communication skills
- Strong literature review and data interpretation abilities
- Attention to detail and strong organizational skills
- Ability to manage multiple documents and meet deadlines
- Proficiency in MS Word, PowerPoint, and literature databases
Job Types: Full-time, Permanent, Fresher
Pay: From ₹25,000.00 per month
Benefits:
- Food provided
- Health insurance
- Paid sick time
- Paid time off
- Provident Fund
Ability to commute/relocate:
- Bengaluru, Karnataka: Reliably commute or planning to relocate before starting work (Required)
Education:
Language:
- English (Required)
- Kannada (Preferred)
- Hindi (Preferred)
Shift availability:
Work Location: In person
