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Parexel Hiring Medical Writer I, II, Senior & Principal Medical Writer – Patient Safety
🏢 Parexel
📍 Bengaluru & Hyderabad
🌍 Remote Opportunities
🛡️ Pharmacovigilance
🎓 0–8+ Years
Parexel is hiring multiple Medical Writing professionals for Patient Safety & Pharmacovigilance roles in India.
These opportunities are ideal for candidates interested in Medical Writing, Aggregate Safety Reports, Pharmacovigilance, Signal Detection, Risk Management Plans, Drug Safety, and Regulatory Writing.
📋 Parexel Hiring Overview
- Company: Parexel
- Roles: Medical Writer I, Medical Writer II, Senior Medical Writer, Principal Medical Writer
- Department: Patient Safety / Pharmacovigilance
- Location: Bengaluru, Hyderabad & Remote
- Job Type: Full-Time
- Experience: 0–8+ Years
- Last Date to Apply: 31 May 2026
💰 Estimated Salary Range: ₹4 – ₹22 LPA
🏢 About Parexel
Parexel is one of the world’s leading Clinical Research Organizations (CROs), supporting pharmaceutical, biotechnology, and medical device companies with Clinical Research, Regulatory Affairs, Pharmacovigilance, and Medical Writing services globally.
The organization provides strong global exposure, flexible remote opportunities, international client interaction, and long-term career growth in Drug Safety and Regulatory Writing domains.
🧾 Medical Writer I – Patient Safety
💰 Estimated Salary: ₹4 – ₹7 LPA
🎓 Qualification
- B.Pharm / M.Pharm / Pharm.D
- BSc / MSc Life Sciences
- Biotechnology / Microbiology / Biomedical Sciences
🧑💻 Experience Required
- 0–2 Years
📌 Key Responsibilities
- Assist in aggregate safety report preparation
- Support PSURs, PBRERs, and DSUR documentation
- Review literature and safety data
- Support signal detection activities
- Coordinate with global PV teams
⭐ Required Skills
- Basic Pharmacovigilance knowledge
- Medical Writing interest
- Scientific communication skills
- Attention to detail
- MS Office proficiency
📚 Medical Writing & PV Resources
👉 Entry-Level Pharmacovigilance Quiz
👉 Top 100 Pharmacovigilance Interview Questions
👉 Pharmacovigilance Salary Guide
📄 Medical Writer II – Patient Safety
💰 Estimated Salary: ₹7 – ₹11 LPA
🎓 Qualification
- B.Pharm / M.Pharm / Pharm.D
- Life Sciences / Biotechnology
🧑💻 Experience Required
- 2–5 Years
📌 Key Responsibilities
- Prepare aggregate safety reports independently
- Handle signal detection and safety evaluations
- Support Risk Management Plans (RMPs)
- Review safety databases and scientific literature
- Coordinate regulatory submission activities
⭐ Required Skills
- Aggregate safety report writing
- MedDRA & WHO-DD knowledge
- Signal management experience
- Global PV regulations understanding
- Project coordination abilities
📚 Advanced PV Resources
👉 Regulatory Affairs vs Pharmacovigilance
👉 Drug Safety Analyst Quiz
👉 Explore Knowledge Hub
🛡️ Senior Medical Writer – Patient Safety
💰 Estimated Salary: ₹12 – ₹18 LPA
🎓 Qualification
- M.Pharm / Pharm.D / MSc Life Sciences
- Biomedical Sciences / Biotechnology
🧑💻 Experience Required
- 5–8 Years
📌 Key Responsibilities
- Lead aggregate report writing activities
- Perform advanced safety analysis and signal evaluation
- Review Risk Management Plans and safety narratives
- Support audits and inspection readiness
- Mentor junior medical writers
⭐ Required Skills
- Advanced Medical Writing expertise
- Leadership and mentoring abilities
- Strong safety analysis experience
- Regulatory compliance expertise
- Client communication skills
📚 Career Growth Resources
👉 Clinical Research Career Guide
👉 Healthcare IT vs Clinical Healthcare
👉 Explore Healthcare Quizzes
🌍 Principal Medical Writer – Patient Safety
💰 Estimated Salary: ₹18 – ₹22+ LPA
🎓 Qualification
- M.Pharm / Pharm.D / MSc / Biomedical Sciences
🧑💻 Experience Required
- 8+ Years
📌 Key Responsibilities
- Lead global pharmacovigilance writing projects
- Handle complex aggregate safety submissions
- Support global regulatory strategy discussions
- Guide cross-functional PV and regulatory teams
- Ensure inspection readiness and compliance
⭐ Required Skills
- Strategic safety writing expertise
- Global pharmacovigilance regulations
- Leadership & stakeholder management
- Advanced aggregate reporting experience
- Regulatory submission expertise
📚 Leadership & Interview Resources
👉 Pharma & Healthcare Interview Questions
👉 Aptitude & Reasoning Quiz
👉 Explore HiTechPlus
🌍 Benefits of Working at Parexel
- Global CRO exposure
- Remote & Hybrid opportunities
- Career growth in Medical Writing & Pharmacovigilance
- International project exposure
- Learning and development programs
- Collaborative global teams
- Exposure to global safety regulations
📄 Resume & Interview Tips
- Highlight aggregate report writing experience
- Mention MedDRA, WHO-DD, and safety database exposure
- Add signal management & RMP experience
- Showcase scientific writing skills clearly
- Keep resume ATS-friendly and achievement-focused
🎯 Interview Preparation Resources
👉 Clinical Trial Assistant Quiz
👉 CRA Quiz & Clinical Research Practice
👉 Explore Latest Medical Jobs
🚀 Select Role & Apply
📌 Note Before You Apply:
We use a 15-second timer to encourage candidates to carefully review the selected role before applying. Understanding the responsibilities and requirements improves your chances of selection and creates a strong professional impression.
We use a 15-second timer to encourage candidates to carefully review the selected role before applying. Understanding the responsibilities and requirements improves your chances of selection and creates a strong professional impression.
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