Are you a life sciences graduate looking to break into the world of Medical Writing? 🧪 If you’re passionate about clinical research, toxicology, and regulatory documentation, this is the perfect launchpad for you.
Cencora (formerly AmerisourceBergen), a global leader in healthcare solutions, is inviting applications for the role of Trainee Specialist – CLS Global Medical Writing at their Noida hub.
This is a golden opportunity for freshers to join a global consulting ecosystem (affiliated with PharmaLex India division) and contribute to projects that truly create healthier futures. 🌍
🏢 About Cencora – Why Join?
Cencora is a purpose-driven organization united by its mission to create healthier futures. With its strategic expansion in India, especially in regulatory consulting and global medical writing, the Noida hub is becoming a strong center for EU and international regulatory projects.
For a fresher, this means:
✔ High-quality mentorship
✔ Exposure to EU Marketing Authorization procedures
✔ Strong regulatory documentation training
✔ Inclusive and Equal Opportunity work culture 🤝
📝 Job Profile Overview
- Role: Trainee Specialist, CLS Global Medical Writing
- Location: Noida, India 📍
- Employment Type: Full-time ⏰
- Category: Consulting
- Company: Cencora (PharmaLex Division)
- Job ID: R26160
🎯 Key Responsibilities
As a Trainee Specialist, you’ll build core regulatory expertise:
📚 Systematic Literature Searches
- Conduct structured searches in PubMed, Google Scholar, and scientific databases
- Extract evidence-based data for regulatory documentation
💊 Marketing Authorization Dossiers
- Assist in drafting pre-clinical and clinical sections
- Support EU and international regulatory submissions
🧪 Toxicology Assessments
- Work on PDE (Permitted Daily Exposure)
- Contribute to OEL (Occupational Exposure Limit) reports
- Gain rare and high-demand toxicology documentation skills
📈 Medico-Marketing Materials
- Help prepare product rationales, publications, and regulatory-backed marketing documents
✅ Eligibility Criteria
Cencora seeks focused, responsible, and quality-driven candidates.
🎓 Educational Background
- M.Pharm / MSc / PhD in Pharmacy, Life Sciences, Pharmacology, or Toxicology
💻 Technical Skills
- Excellent MS Office skills (Word, Excel, PowerPoint)
- Comfortable with literature databases (PubMed, Google Scholar)
📖 Knowledge Advantage
- Basic understanding of EU marketing authorization
- Familiarity with regulatory documentation principles
🗣 Language Skills
- Exceptional written and verbal English (non-negotiable for medical writing roles)
🤝 Soft Skills
- Detail-oriented mindset
- Ability to work independently and within teams
🎁 What’s in It for You?
🌐 Global exposure to EU and international projects
📈 Clear career progression (Trainee → Specialist → Senior Consultant)
🤝 Inclusive, non-discriminatory culture
💼 Strong consulting profile for long-term growth
For someone starting in Regulatory Affairs or Medical Writing, this is a prestigious entry point.
💡 Pro Tips for Your Application
Since you’re building your freelance writing profile as well, Parag, this role perfectly aligns with your writing strength. Highlight that advantage smartly:
✔ Mention any thesis, dissertation, or literature review work
✔ Emphasize structured writing and analytical ability
✔ Keep your CV completely typo-free
✔ In your cover letter, connect with their purpose:
“I am motivated to contribute toward creating healthier futures through evidence-based medical documentation.”
🏁 Final Thoughts
Noida is a fast-growing hub for regulatory and pharmacovigilance careers. Starting with Cencora’s Global Medical Writing team can put you on a high-growth international career track. 🚀
Opportunities like this in consulting fill fast — apply as soon as possible.
🔗 Apply Here:
https://careers.cencora.com/us/en/job/R26160/Trainee-Specialist-CLS-Global-Medical-Writing
