To develop high-quality scientific content and documentation across therapeutic areas by conducting in-depth literature reviews, synthesizing data, and delivering clear, accurate, and audience-appropriate materials.
The role involves contributing to both short- and long-term projects in the consumer healthcare and pharmaceutical sectors, including medical, safety, pre-clinical, clinical, regulatory, educational, and promotional content.
Additional responsibilities include editing, proofreading, reviewing, referencing, and verifying content to ensure adherence to high medical writing standards.
The role ensures timely delivery of project milestones while maintaining quality, compliance, and business value.
MBBS / BDS / PhD / Master’s in Pharmacy or a related field
Immediate joiners