Analyst Job at Norstella | Remote Opportunity for Medical Graduates
Looking for an analyst job in the medical industry? Norstella is hiring an Analyst I, Drugs for a remote job in India. This exciting opportunity under Norstella careers allows professionals with experience in pharmaceutical research and data analysis to work with a global leader in AI-driven healthcare intelligence. If you have expertise in drug development processes, regulatory pathways, and secondary data analysis, this remote job could be your next big career move.
Job Details:
- Job Position: Analyst I, Drugs
- Company: Norstella
- Location: Remote, India
- Job ID: R-1726
About the Company:
Norstella is a premier and critical global life sciences data and AI solutions provider dedicated to improving patient access to life-saving therapies. The company supports pharmaceutical and biotech organizations across the full drug development lifecycle — from pipeline to patient. Norstella unites market-leading brands. Through AI-powered insights and proprietary data, Norstella helps pharmaceutical and biotech companies. Norstella also serves regulators such as the U.S. Food and Drug Administration and global payers. Investments in AI are transforming how healthcare data is consumed, enabling faster and more confident decision-making. This makes Norstella careers highly attractive for professionals seeking innovation-driven roles.
Job Description:
This analyst job involves managing complex pharmaceutical data workflows, ensuring high-quality content delivery, and contributing to quality assurance and process improvements. The Analyst I role includes secondary research, stakeholder coordination, and internal reporting to support Norstella’s mission of delivering actionable pharmaceutical intelligence. This remote job offers the opportunity to work at the intersection of AI, drug development, and healthcare data analytics.
Qualifications:
- Graduate/Post-Graduate/Doctorate degree in Medical Sciences or equivalent field
- Minimum 3 years of work experience in business research and secondary data analysis, preferably in life sciences or healthcare
- Strong understanding of drug development processes, MoAs, indications, and regulatory pathways
- Experience using research tools and databases such as ClinicalTrials.gov, EMA, FDA, and SEC filings
- High proficiency in MS Office Suite (Excel, Word, PowerPoint)
- Strong analytical and reporting skills
Key Responsibilities:
- Identify and extract key drug data from public sources such as clinical trial registries, regulatory filings, and company reports
- Assess and track drug pipelines by stage, indication, and mechanism of action (MoA)
- Interpret MoAs and connect them to disease pathways and clinical outcomes
- Track regulatory designations and approvals (e.g., Orphan Drug, Breakthrough Therapy)
- Validate and cross-check data entries across multiple sources for accuracy
- Apply business rules, SOPs, and publishing workflows effectively using Fusion
- Meet daily and weekly productivity targets while ensuring data quality
- Manage multiple research tasks efficiently while maintaining quality and turnaround time
