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Tier-1 pharma brand, metro location, mid-level generalist analytics role, broad tech stack.
Role requires pharma REMS and regulatory safety analytics domain expertise, limiting cross-industry transferability.
Explicit 5–8 years, REMS/regulatory domain expertise, and mandatory tech stack increase filter strictness.
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Develop and maintain data analytics reporting frameworks and visualizations for Worldwide Patient Safety & Pharmacovigilance (PV) analytics, focusing on BMS REMS & Clinical Analytics.
Analyze compliance data and key metrics to provide insights on productivity, efficiency, quality, and regulatory adherence, supporting informed decision-making and audit activities.
Collaborate cross-functionally to interpret data findings, respond to stakeholder issues, and present actionable reports and studies to management and leadership regularly.
Bachelor’s degree required (Master’s or advanced degree preferred).
At least 5 - 8 years of relevant pharma/biotech experience with understanding of FDA Risk Evaluation and Mitigation Strategies (REMS).
Proficiency with data visualization tools (Tableau, Spotfire), programming languages (SAS, SQL, Python), and databases (Salesforce, Postgres, Oracle).
Strong skills in PowerPoint, Excel, and knowledge of clinical and real-world data analysis; ability to support audit activities.
Experienced in handling regulatory compliance and drug safety data analytics in pharmaceutical or biotech environments.
Strategic thinker capable of translating data insights into operational priorities and actionable recommendations.
Skilled at managing multiple projects and collaborating with cross-functional teams including Regulatory, Medical, Clinical Safety, and Commercial functions.