Gaint Global Pharma Company

The Role

Key Responsibilities

• Content Development: Write, edit, and proofread a variety of medical and scientific documents, including clinical study reports, regulatory submissions, journal articles, abstracts, posters, white papers, and more.
• Research: Conduct comprehensive literature reviews and gather relevant information from various scientific sources to support content development.
• Compliance: Ensure all written materials comply with regulatory guidelines, company standards, and industry best practices.
• Collaboration: Work closely with cross-functional teams including medical affairs, regulatory affairs, marketing, and subject matter experts to gather information and ensure the accuracy and relevance of content.
• Data Interpretation: Analyze and interpret complex clinical data, and present it clearly and concisely in various formats.
• Project Management: Manage multiple writing projects simultaneously, ensuring timely delivery of high-quality content.
• Quality Assurance: Participate in the quality control process by reviewing materials for scientific accuracy, consistency, and grammar.
• Training and Development: Stay current with industry trends and best practices and provide training or mentorship to junior writers if applicable.
  
  

Ideal Profile

2 to 8 years

Medical writing experience in Abstract, Poster, Manuscript - Diabetics/ Oncology/NeuroScience

Bangalore - working 3 days from Office - should be willing to relocate

What's on Offer?

• Flexible working options
• Fantastic work culture
• Opportunity to make a positive impact