Medical Writer Job | Novaspire Biosciences Careers

Novaspire Biosciences, a trusted partner in the pharmaceutical industry, is hiring a Medical Writer in Bengaluru, Karnataka. If you have a passion for scientific writing and medical communications, this full-time, on-site role offers the opportunity to craft high-quality clinical and regulatory documents while collaborating with cross-functional teams in the pharmaceutical and biotechnology sectors.

Key Responsibilities

As a Medical Writer at Novaspire Biosciences, you will:

• Write, edit, and review clinical and regulatory documents including:
  • Protocols and Amendments
  • Investigator Brochures
  • Informed Consent Documents
  • Case Report Forms (CRFs)
  • Clinical Study Reports (CSRs)
  • Common Technical Document (CTD) modules (e.g., 2.5, 2.7) – optional
• Develop scientific content for publications, abstracts, posters, slide decks, and white papers.
• Ensure compliance with ICH-GCP guidelines, regulatory requirements (FDA, EMA), and internal SOPs.
• Accurately interpret clinical and scientific data and present it clearly to varied audiences.
• Collaborate effectively with clinical, regulatory, pharmacovigilance, and biostatistics teams.
• Maintain version control, adhere to timelines, and ensure quality across all documents.
• Prepare and review medical writing SOPs and provide training as required.
• Participate in client-specific medical writing activities and provide strategic guidance on document planning.

Qualifications

• Bachelor’s or Master’s degree in Life Sciences, Medicine, Pharmacy, or equivalent.
• Strong scientific writing and medical writing skills.
• Proficiency in medical communications and general writing.
• Strong research abilities and excellent written/verbal communication skills.
• Ability to work independently and collaboratively with diverse teams.
• Experience in pharmaceutical or healthcare industries is a plus.

Benefits

• Opportunity to work with a leading pharmaceutical research and consulting company.
• Exposure to clinical trials, pharmacovigilance, and regulatory documentation.
• Collaborative environment with opportunities for professional growth.
• Hands-on experience with high-quality scientific publications and GxP compliance.

How to Apply

Application Link