Research Job Opportunity at Nortsella | Apply Now for Pharma Job (Remote India)
If you are searching for Research Jobs and Pharma Jobs in the life sciences industry, this opportunity at Norstella could be the perfect fit. The Researcher, Drugs role is a full-time remote position in India focused on structured secondary research, regulatory intelligence, and high-quality drug data development. This role directly supports pharmaceutical innovation and accelerates patient access to life-saving therapies.
- Job Title: Researcher, Drugs
- Location: Remote, India
- Job ID: R-1723
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. Norstella supports pharmaceutical and biotech companies across the full drug development lifecycle — from pipeline to patient. Our mission is simple: to help our clients bring therapies to market faster and more efficiently, ultimately impacting patient lives.
Norstella unites market-leading brands – Citeline, Evaluate, MMIT, Panalgo, Skipta and The Dedham Group and delivers must-have answers and insights, leveraging AI, for critical strategic, clinical, and commercial decision-making.
Job Description
The Researcher supports the creation of high-quality drug intelligence content by conducting structured secondary research, extracting regulatory and clinical information, and ensuring data integrity. This role plays a key part in developing reliable pharma R&D content for Norstella’s platforms, contributing to our mission of accelerating access to life-saving therapies.
Key Responsibilities
- Identify and extract key drug data from public sources (e.g., clinical trial registries, regulatory filings, company report)
- Demonstrate working knowledge of FDA, EMA, and other global regulatory agencies’ processes
- Apply foundational knowledge of therapeutic areas and mechanisms of action (MoAs) to drug research
- Adhere to SOPs and gather information from source publishing processes.
- Check and validate content for accuracy and basic errors before submission
- Meet daily and weekly productivity targets while ensuring data quality
- Develop proficiency in authoring tools and extensions to support publishing
Qualifications
- Graduate/Post-Graduate/Doctorate in Pharmacy or a related discipline
- Minimum 1 year of experience in pharmaceutical research, clinical data, or drug content development preferred
- Understanding of regulatory databases (e.g., ClinicalTrials.gov, EMA, FDA) and public data sources
- Familiarity with drug development lifecycle, therapeutic areas, and MoAs
- Proficient in MS Office Suite, especially Excel and Word.
Benefits
- Health Insurance
- Provident Fund
- Life Insurance
- Reimbursement of Certification Expenses
- Gratuity
- 24×7 Health Desk
