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Alvotech Hiring For Medical Writer

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Alvotech

MSc / PhD / PharmD / MD in Life Sciences

Bangalore

3 - 5 years

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Alvotech is hiring an experienced Medical Writer (Pharmacovigilance & Clinical Writing) for its Bangalore and remote India locations. This is an excellent opportunity for professionals with strong expertise in clinical development, pharmacovigilance writing, and regulatory documentation.

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Alvotech, a leading biosimilar pharmaceutical company, is expanding its Integrated Clinical and Medical Research (iCMR) team. If you have 5+ years of experience in medical writing across clinical and post-marketing stages, this role offers strong career growth in global regulatory environments.


📌 Job Overview – Medical Writer (Alvotech India)

  • Company: Alvotech
  • Job Title: Medical Writer
  • Location: Bangalore Office / India (Partially Remote)
  • Job Type: Full-Time
  • Last Date to Apply: March 31, 2026
  • Department: Clinical & Medical Research (iCMR)

🧪 Key Responsibilities

As a Medical Writer in pharmacovigilance and clinical research, you will:

  • Lead preparation of clinical trial protocols, amendments, and CSRs (Clinical Study Reports)
  • Develop pharmacovigilance documents including safety reports and risk-benefit analyses
  • Write regulatory submission documents aligned with global guidelines (ICH, GCP)
  • Support post-marketing scientific publications and safety documentation
  • Collaborate with Clinical Development, Biostatistics, and PV teams
  • Ensure timely document delivery and compliance with regulatory standards
  • Translate complex clinical and safety data into clear, accurate scientific content

🎓 Qualifications & Experience

To qualify for this Medical Writer job in India, candidates must have:

  • MSc / PhD / PharmD / MD in Life Sciences or related field
  • Minimum 5 years of medical writing experience across product lifecycle
  • At least 3 years in pharmacovigilance writing
  • Strong understanding of GCP, ICH guidelines, and global PV regulations
  • Experience in clinical trials, CSRs, IBs, and regulatory submissions
  • Excellent scientific writing, data interpretation, and communication skills
  • Experience in biosimilars (preferred)
  • Ability to work in multicultural, cross-functional teams

💼 Why Join Alvotech?

  • Work with a global biosimilar leader
  • Exposure to end-to-end product lifecycle writing
  • Opportunity to contribute to regulatory submissions worldwide
  • Flexible remote + office work model in India
  • Collaborative and innovation-driven R&D environment

📄 How to Apply

Application Link

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