Job Description

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 1+ 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: ?25,000.00 - ?35,000.00 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:

Doctorate (Preferred)
Language:

English (Required) Kannada (Preferred) Hindi (Preferred)
Shift availability:

Day Shift (Required)
Work Location: In person