Posted:4 weeks ago|
Platform:
On-site
Full Time
Specialized in pharmaceutical research and competitive intelligence, with expertise in drug development, clinical trial analytics, and regulatory insights — delivering accurate data.
Conduct secondary research on drugs, mechanisms, targets, and indications; track innovative drug pipelines, regulatory updates, and clinical trials.
Analyze, maintain, and validate pharmaceutical databases with accuracy on key fields such as drug names, MOA, sponsors, molecule types, and trial data.
Monitor developments from regulatory bodies (US FDA, EMA, CDE, etc.), industry reports, patents, and company filings to provide usable and intellectual data.
Prepare weekly/monthly reports, databooks, and dashboards; deliver strategic recommendations on training the team on accurate data capture and address client queries.
Collect and analyze information from trial registries, filtering by condition, intervention, phase, and recruitment status; capture critical study details such as endpoints, design, inclusion/exclusion criteria, and sponsor information.
Identify tool/process gaps, ensure compliance with company guidelines, and support capability building through training and knowledge sharing to enhance team performance.
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