Management Trainee - Life Science

Roles & Responsibilities
• Gather and integrate data from multiple sources such as medicinal product information reports and licensing records
• Transcribe and update product information into client-supported databases and tools
• Perform accurate coding of medicinal products using standardized terminology (MedDRA – Medical Dictionary for Regulatory Activities)
• Ensure adherence to regulatory compliance requirements and predefined SLAs
• Identify data gaps and coordinate with teams to resolve discrepancies
• Maintain high standards of quality, accuracy, and timely delivery
• Ensure confidentiality of sensitive client and regulatory information
• Follow Escalent and client Standard Operating Procedures (SOPs)

Qualification
• Biotechnology

Experience
• 0–1 year of relevant work experience
• Freshers with strong medical terminology knowledge may apply

Skills
• Strong attention to detail and data accuracy
• Knowledge of medical terms and regulatory terminology
• Familiarity with MedDRA coding preferred
• Good time management and ability to meet daily deadlines
• Strong written and verbal communication skills
• Ability to work in different shifts (no night shifts)
• Professional problem-solving approach and integrity

About the Organization
Escalent is an award-winning data analytics and advisory firm with over 40 years of experience, helping global brands navigate market disruption through advanced research, regulatory support, and data-driven insights across industries including pharmaceuticals.