STEM Content Analyst – Clarivate, (SQL, Python, GenAI)

Clarivate is seeking a STEM Content Analyst to join its CDDI Drugs team in Hyderabad, India. This hybrid role offers an exciting opportunity to work on drug development research, competitive analysis, pipeline evaluation, and regulatory information analysis. Ideal for M.Pharm, B.Pharm, or D.Pharm professionals with 2+ years of experience in secondary market research and content analysis.

The role is perfect for detail-oriented individuals passionate about drug development, clinical trials, and pharmaceutical research. You’ll collaborate with colleagues in India and Spain, contributing to structured drug summaries and insightful content for external scientists.

Key Responsibilities

• Analyze drug-based references including clinical trials, press releases, regulatory updates (FDA, EMA).
• Identify new drugs, development phases, target diseases, formulations, and organizations involved in drug research.
• Summarize and edit reference information accurately, maintaining clarity and conceptual correctness.
• Conduct comprehensive online research to find relevant drug references.
• Consistently meet weekly production and quality targets while achieving KPI metrics.
• Actively participate in team discussions and process improvement initiatives.
• Collaborate with ROW & Cross BU groups on-demand and adapt to process changes.
• Perform tasks assigned by line managers or directors, both permanent and temporary.

Qualifications

Mandatory:

• M.Pharm, B.Pharm, or D.Pharm degree.
• Minimum 2 years of experience in secondary market research, competitive analysis, or related pharmaceutical research.
• Strong content analysis and editing skills.
• Excellent written and oral communication skills.
• Proficient in Microsoft Word, Excel, and PowerPoint.
• Ability to work independently and in a team, adhering to SOPs and company policies.

Preferred (Optional):

• Familiarity with AI tools in research and analysis.
• Knowledge of SQL or Python for data handling and reporting.

Benefits

• Opportunity to work with a global drug development team.
• Exposure to clinical trial analysis, regulatory affairs, and pharmaceutical pipelines.
• Collaborative and innovative work environment with hybrid flexibility.
• Professional growth and learning opportunities in the pharmaceutical and biotech industry.

How to Apply

Application Link