Trainee Specialist CLS Global Medical Writing

Roles & Responsibilities:
• Perform systematic literature searches for regulatory and scientific documents
• Assist in preparing pre-clinical and clinical sections of Marketing Authorization Dossiers (CTD/eCTD)
• Support toxicology documentation including PDE, OEL, and other risk assessments
• Contribute to medical-scientific documents such as publications, product rationales, and medico-marketing materials
• Collaborate closely with senior medical writers and regulatory managers
• Handle additional responsibilities aligned with role capabilities

Qualification:
• Degree in Pharmacy, Life Sciences, or related discipline

Experience:
• Freshers

Skills:
• Strong interest in medical writing and regulatory affairs
• Basic understanding of EU marketing authorization procedures
• Awareness of economic principles related to healthcare/pharma
• Excellent written and spoken English communication skills
• Proficiency in MS Word, Excel, PowerPoint, and scientific literature review
• Ability to work independently with high accuracy and attention to detail
• Strong teamwork, responsibility, and interpersonal skills

About The Company:
Cencora offers global exposure in regulatory medical writing. The company provides structured training and mentorship for early-career professionals, working on international regulatory submissions. With a commitment to an inclusive and equal opportunity workplace, Cencora offers competitive compensation and long-term career growth opportunities within its global ecosystem.