Senior Researcher / Associate Analyst

Roles & Responsibilities
• Conduct extensive secondary research on drug development pipelines and clinical trials
• Analyze regulatory approvals, patent landscapes, and pharmaceutical manufacturer data
• Research drug sales, forecasting trends, biomarkers, and investigator databases
• Study chemical and biological drugs across multiple therapy areas
• Review global regulatory frameworks (USFDA, EMA, CDSCO, etc.)
• Extract and analyze data from pharmaceutical databases and public sources
• Prepare structured analytical reports using MS Excel and Word
• Work across different therapy domains as per project requirements

Qualification
• M.Pharm (Pharmaceutical Chemistry / Regulatory Affairs / Pharmacology / Pharmaceutics)
• Pharm.D
• Candidates who passed out within the last two years

Experience
• Freshers eligible to apply
• Strong academic exposure to drug development and regulatory concepts preferred

Skills
• Strong analytical and critical thinking abilities
• Knowledge of drug discovery and development process
• Understanding of clinical trial phases (I–IV)
• Familiarity with global regulatory bodies and compliance frameworks
• Proficiency in MS Excel and MS Word
• Strong written and verbal communication skills
• Ability to manage multiple assignments with attention to detail

About the Organization
GlobalData is a leading global analytics and research firm providing data-driven insights to the healthcare and pharmaceutical industries, supporting strategic decision-making across drug development, clinical intelligence, and market research domains.