Full Time

Pharmaceutical Research - Drugs

Norstella
Remote, India
Competitive Salary
Posted 17/02/2026

About the Role

Roles & Responsibilities:
• Extract structured drug data from public sources like Clinical Trials gov, regulatory filings, and company reports
• Analyze regulatory submissions from FDA, EMA, and other global agencies
• Apply knowledge of therapeutic areas and mechanisms of action (MoAs)
• Follow SOPs to maintain structured publishing workflows
• Validate regulatory and clinical data for accuracy and completeness
• Meet productivity targets while maintaining high data integrity
• Use internal authoring tools for pharma R&D content development

Qualification:
• Bachelor of Pharmacy (B.Pharm)
• Master of Pharmacy (M.Pharm)
• Doctor of Pharmacy (Pharm.D)
• Graduate / Postgraduate / Doctorate in Life Sciences, Pharmacy, or Medical Sciences

Experience:
• Minimum 1 year experience in pharmaceutical research or clinical data

Skills:
• Understanding of regulatory databases (FDA, EMA, Clinical Trials gov)
• Knowledge of drug development lifecycle and therapeutic areas
• Strong MS Excel & Word proficiency
• Experience in clinical trial data extraction, drug pipeline intelligence, regulatory database research, or pharmaceutical content development

About the Organization:
Norstella is a global life sciences data and AI solutions provider supporting pharmaceutical and biotech companies across the entire drug development lifecycle — from pipeline to patient access.

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