Fresher Trainee Medical Writing Jobs at Cencora
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- SEO-Focused Job Title Variations
- Summary Table
M Pharmacy, Life Sciences Jobs at Cencora | Trainee Medical Writing – Noida
Cencora hiring Trainee Specialist – CLS Global Medical Writing in Noida. Pharmacy and life sciences graduates eligible. Full-time role.
Cencora is inviting applications for the role of Trainee Specialist – CLS Global Medical Writing at its Noida location. This position is designed for early-career professionals who want to build a strong foundation in regulatory medical writing, scientific documentation, and global marketing authorization processes. The role offers hands-on exposure to regulatory dossiers, toxicology documentation, and medical-scientific content within a structured global consulting environment.
Company Overview
Cencora is a global healthcare services organization committed to creating healthier futures for people and animals worldwide. The company operates at the center of health by supporting pharmaceutical, biotech, and healthcare organizations through regulatory consulting, medical writing, clinical development, and commercialization services.
Through its affiliated company, PharmaLex India Private Limited, Cencora provides end-to-end regulatory and scientific support across global markets, including the EU, US, and other international regions. The organization is known for its strong ethical framework, compliance-driven culture, and deep scientific expertise. Working at Cencora means contributing directly to regulatory excellence and patient safety on a global scale.
Job Role & Responsibilities
The Trainee Specialist – CLS Global Medical Writing role focuses on supporting regulatory and medical writing activities under the guidance of experienced managers and subject matter experts. This role plays a key part in the preparation of high-quality scientific and regulatory documents used in global marketing authorization submissions.
Key Responsibilities
• Perform systematic literature searches for regulatory, clinical, and scientific documents • Support managers in preparing pre-clinical and clinical sections of marketing authorization dossiers • Assist in the development of toxicology assessments such as PDE, OEL, and related safety documents • Contribute to the preparation of medical-scientific documents including publications, product rationales, and medico-marketing materials • Review and organize scientific literature to support regulatory strategies • Ensure accuracy, consistency, and compliance with regulatory guidelines • Take on additional reasonable tasks aligned with skill level and training requirements • Collaborate closely with cross-functional teams to meet project timelines
This role provides structured exposure to high-CPC career domains such as medical writing jobs, regulatory documentation roles, clinical regulatory support, and pharmaceutical consulting careers.
Eligibility / Qualifications
This role is suitable for candidates with a strong academic foundation in pharmacy, life sciences, or related scientific disciplines who are looking to start a career in medical writing or regulatory consulting.
Required Education
M Pharmacy, B Pharmacy, Pharmaceutics, Pharmacology, Pharmaceutical Analysis, Pharmaceutical Chemistry, Biotechnology, Life Sciences, Clinical Research, Toxicology, Biomedical Sciences or equivalent qualification
Skills & Knowledge
• Strong attention to detail and ability to perform high-quality, focused work • Ability to work both independently and within a team environment • Sense of responsibility and accountability for assigned tasks • Basic understanding of EU marketing authorization procedures • Basic knowledge of economic and healthcare principles • Excellent command of written and spoken English • Strong communication and interpersonal skills • Proficiency in MS Office tools including Word, Excel, and PowerPoint • Familiarity with scientific literature databases and research methodologies
Location & Salary
Job Location: Noida, Uttar Pradesh, India
Application Process
Eligible candidates can apply directly through the official Cencora careers portal. Applications are reviewed on a rolling basis.
Candidates are advised to highlight academic projects, literature review experience, regulatory exposure, and scientific writing skills in their resumes.
Frequently Asked Questions (FAQs)
Q1. Is this role suitable for freshers?
Yes. This is a trainee-level role designed for early-career candidates and fresh graduates.
Q2. What type of documents will I work on?
You will support regulatory dossiers, toxicology assessments, clinical sections, and medical-scientific documents.
Q3. Is prior regulatory experience mandatory?
No. Basic knowledge of regulatory processes is sufficient. Training will be provided.
Q4. Is this a remote role?
No. This is a full-time, on-site position based in Noida.
Q5. Which career paths can this role lead to?
Medical Writer, Regulatory Affairs Specialist, Clinical Documentation Expert, or Regulatory Consultant.
SEO-Focused Job Title Variations
• Cencora Medical Writing Jobs for Freshers • Trainee Medical Writer Vacancy at Cencora Noida • Pharmacy Graduate Medical Writing Jobs • CLS Global Medical Writing Trainee Roles
Summary Table
| Category | Details |
|---|---|
| Company | Cencora (PharmaLex India Private Limited) |
| Vacancies | Trainee Specialist – CLS Global Medical Writing |
| Required Education | M Pharmacy, B Pharmacy, Life Sciences, Biotechnology, Pharmacology, Clinical Research |
| Experience | Fresher / Entry-Level |
To apply for this job please visit careers.cencora.com.
