Associate STEM Content Analyst

Roles & Responsibilities

• Analyse drug development information from clinical trials, regulatory agencies, and scientific sources
• Track new drugs, pipeline updates, development phases, indications, and sponsors
• Perform primary and secondary research on global drug development activities
• Summarize, edit, and validate scientific and pharmaceutical content with high accuracy
• Conduct comprehensive online searches for drug and clinical intelligence
• Maintain assigned production volumes, quality standards, and KPIs
• Collaborate with global teams across regions and business units
• Follow SOPs and contribute to process improvement initiatives
• Adapt to workflow changes in a fast-paced research environment

Qualification

• M.Pharm / B.Pharm / D.Pharm

Experience

• Freshers or up to 6 months of relevant experience

Skills

• Strong understanding of drug development and clinical research concepts
• Excellent written and verbal communication skills
• Good content analysis, summarization, and editing abilities
• Proficiency in MS Word, Excel, and PowerPoint
• Strong attention to detail and time management skills

• Exposure to AI tools for research or content analysis
• Basic knowledge of SQL or Python
• Interest in pharmaceutical analytics, clinical intelligence, and drug pipelines

About the Team

Clarivate’s Drug Development (CDDI) team delivers high-quality intelligence on clinical trials, regulatory pipelines, and drug research, covering MoA, development milestones, regulatory pathways, and disease focus to support global pharmaceutical decision-making.