Alvotech Medical Writer Bangalore Remote Hiring
- Alvotech Hiring Medical Writer (Bangalore/Remote) | 5+ Years Clinical & Pharmacovigilance Writing Role
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Background:
- Experience Required:
- Skills Required:
- Location & Salary
- Application Process
- Why This Role Matters in Healthcare
- Frequently Asked Questions (FAQs)
- 1. Is this role suitable for freshers?
- 2. What documents will I work on?
- 3. Is pharmacovigilance experience required?
- 4. Is this a remote job?
- Summary
Alvotech Hiring Medical Writer (Bangalore/Remote) | 5+ Years Clinical & Pharmacovigilance Writing Role
Looking to grow in high-impact medical writing and regulatory documentation roles? Alvotech is hiring experienced Medical Writers for its Clinical and Medical Research (iCMR) team in Bangalore with partial remote flexibility. This opportunity is ideal for professionals with 5+ years of experience in clinical, regulatory, and pharmacovigilance writing.
This role focuses on end-to-end medical writing across clinical development and post-marketing phases, including clinical study reports, safety documents, and regulatory submissions, making it a premium career opportunity in global pharmaceutical and biotech companies.
Company Overview
Alvotech is a leading global biopharmaceutical company specializing in the development and manufacturing of biosimilar medicines. The company is driven by strong R&D capabilities and focuses on delivering affordable biologic therapies to patients worldwide.
The integrated Clinical and Medical Research (iCMR) function plays a critical role in clinical strategy, safety evaluation, and regulatory submissions, ensuring compliance with global health authority requirements.
Job Role & Responsibilities
As a Medical Writer, you will be responsible for developing high-quality scientific and regulatory documents across the entire product lifecycle.
Key Responsibilities:
- Prepare and review clinical documents including protocols, amendments, and Clinical Study Reports (CSRs)
- Develop safety and pharmacovigilance documents aligned with global regulatory strategies
- Support regulatory submissions by creating scientifically accurate and compliant documentation
- Lead development of Investigator Brochures (IBs), submission dossiers, and safety reports
- Contribute to scientific publications and post-marketing documentation
- Interpret complex clinical and safety data and present it clearly for regulatory authorities
- Collaborate with cross-functional teams including Clinical Development, Biostatistics, and Pharmacovigilance
- Manage document timelines and ensure timely delivery of high-quality outputs
Eligibility / Qualifications
Educational Background:
M.Pharmacy, Pharm.D, MSc, PhD (Life Sciences, Biotechnology, Microbiology, Biochemistry), MD, Life Sciences
Experience Required:
- Minimum 5 years of experience in medical writing or clinical documentation
- At least 3 years of experience in pharmacovigilance-related writing
- Experience across clinical development and post-marketing documentation
- Experience in biosimilar or biologics projects preferred
Skills Required:
- Strong scientific writing and data interpretation skills
- Knowledge of ICH-GCP, pharmacovigilance, and global regulatory guidelines
- Excellent attention to detail and documentation quality
- Strong communication and collaboration abilities
- Experience with document management systems preferred
Location & Salary
- Location: Bangalore, India (Partial Remote)
- Job Type: Full-time
- Salary: High-paying package based on experience
Application Process
Interested candidates can apply through the official Alvotech careers portal:
Apply Here: https://alvotech.wd103.myworkdayjobs.com/Alvotech_Careers/job/Bangalore-Office/Medical-Writer_JR100095
Application Deadline: March 31, 2026
Candidates are encouraged to apply early due to high competition for senior medical writing roles.
Why This Role Matters in Healthcare
Medical Writers play a crucial role in translating clinical and safety data into structured documents that support regulatory approvals and scientific communication. This role directly contributes to bringing safe and effective biosimilar therapies to market.
Working in this position allows professionals to influence global healthcare outcomes through high-quality scientific documentation and regulatory compliance.
Frequently Asked Questions (FAQs)
1. Is this role suitable for freshers?
No, this is a senior-level role requiring at least 5 years of experience in medical writing.
2. What documents will I work on?
You will work on Clinical Study Reports (CSRs), protocols, Investigator Brochures, safety documents, and regulatory submissions.
3. Is pharmacovigilance experience required?
Yes, at least 3 years of pharmacovigilance writing experience is required.
4. Is this a remote job?
This is a partially remote role based in Bangalore.
Summary
| Category | Details |
|---|---|
| Company | Alvotech |
| Vacancies | Medical Writer |
| Required Education | M.Pharmacy, Pharm.D, MSc, PhD, MD |
| Experience | 5+ years |
To apply for this job please visit alvotech.wd103.myworkdayjobs.com.
