Career Opportunity: Medical Writer (3-4 Yrs)

Role Summary:
We are seeking a skilled and detail-oriented Medical Writer with 3-4 years of experience and an M.Sc. degree to join our dynamic team in Hyderabad. The Medical Writer will be responsible for creating, reviewing, and editing high-quality scientific and regulatory documents. This role requires a strong understanding of pharmaceutical R&D, regulatory guidelines, and the ability to translate complex scientific information into clear, concise, and accurate content.

Key Responsibilities:
- Prepare, write, and edit various regulatory documents, including Investigator's Brochures (IBs), Clinical Study Reports (CSRs), Common Technical Documents (CTDs), and summaries.
- Ensure all documents comply with relevant regulatory guidelines (e.g., ICH, FDA, EMA) and company SOPs.
- Collaborate with cross-functional teams, including R&D scientists, clinicians, regulatory affairs specialists, and statisticians, to gather information and ensure scientific accuracy.
- Review and edit documents written by other team members for clarity, consistency, and accuracy.
- Manage multiple projects simultaneously, ensuring timely delivery of all assigned tasks.
- Stay updated with the latest scientific advancements and regulatory requirements in the pharmaceutical industry.
- Contribute to the development and maintenance of style guides and templates for medical writing.