Associate STEM Content Analyst

Roles & Responsibilities
• Maintain and update clinical trials databases with accurate and validated information
• Analyze and cross-reference data from trial registries, scientific conferences, press releases, and research publications
• Track pharmaceutical drug pipelines and monitor clinical development phases
• Interpret complex clinical studies and drug-related data
• Perform secondary research related to clinical and pharmaceutical intelligence
• Ensure high data accuracy within clinical trial intelligence platforms
• Deliver weekly productivity and quality targets
• Validate and standardize clinical information for structured database entry
• Support ongoing enhancements to clinical intelligence workflows
• Collaborate with internal teams to maintain data integrity and reporting standards

Qualification
• B.Pharm (Bachelor of Pharmacy)
• M.Pharm (Master of Pharmacy)
• M.Sc (Biotechnology / Microbiology)

Experience
• Fresher or up to 6 months of experience in clinical report analysis or clinical data updating
• Exposure to secondary research in clinical or pharmaceutical domains (preferred)

Skills
• In-depth understanding of clinical trials and drug development phases
• Knowledge of pharmaceutical drug pipelines
• Strong analytical and problem-solving skills
• Excellent written and verbal English communication
• High attention to detail and data accuracy
• Ability to interpret complex clinical and regulatory information

About the Organization
Clarivate provides trusted insights and analytics across life sciences, healthcare, academia, and intellectual property sectors. Through platforms such as Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence, Clarivate delivers comprehensive clinical and drug development data to support pharmaceutical research, competitive intelligence, and strategic decision-making.