Trainee Specialist - CLS Global Medical Writing

Roles & Responsibilities
• Conduct systematic literature searches for regulatory and scientific documentation
• Assist in preparing pre-clinical and clinical sections of CTD/eCTD dossiers
• Support toxicology documentation including PDE, OEL, and risk assessments
• Contribute to medical-scientific documents such as publications, product rationales, and medico-marketing materials
• Collaborate with senior medical writers and regulatory managers on global projects
• Ensure accuracy, compliance, and timely delivery of documentation
• Support additional tasks aligned with medical writing and regulatory functions

Qualification
• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related discipline

Experience
• Freshers or entry-level candidates with strong interest in medical writing and regulatory affairs
• Basic understanding of EU marketing authorization procedures preferred

Skills
• Strong scientific writing and literature review skills
• Knowledge of CTD/eCTD documentation structure
• Understanding of toxicology concepts and healthcare regulations
• Proficiency in MS Word, Excel, and PowerPoint
• Excellent written and spoken English communication
• High attention to detail, analytical thinking, and teamwork ability

About the Organization
Cencora, through PharmaLex India Private Limited, is a global leader in regulatory and medical services, supporting pharmaceutical and biotech companies worldwide. The organization offers strong learning opportunities, global exposure, and structured career growth in medical writing and regulatory affairs.