Senior Epidemiologist, Inflammation, RWE & Regulatory Strategy

🔥 49 minutes ago

🗽 New York, North Carolina, +2 more states – Remote

🗽 New York – Remote 🌲 North Carolina – Remote 🍂 Massachusetts – Remote 🔔 Pennsylvania – Remote

💵 $109.2k - $273k / year

⏰ Full Time

🟠 Senior

🚔 Compliance

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

⚕️ Healthcare Insurance

🧬 Biotechnology

🤖 Artificial Intelligence

💰 $1G Post-IPO Debt on 2023-05

Healthcare Insurance • Biotechnology • Artificial Intelligence

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Support a Real World Evidence team focused on Inflammation, with flexibility across indications (e.g., lupus, IBD, Crohn’s). • Design and execute real-world evidence (RWE) studies that inform clinical development strategy. • Generate evidence to address regulatory questions related to safety profiles and evidence gaps for Phase 2 and Phase 3 programs. • Provide scientific oversight across complex observational research, leveraging secondary data sources such as commercial real-world data platforms. • Apply epidemiologic expertise to study design, execution, and interpretation, focusing on fit-for-purpose evidence for regulatory and clinical decision-making. • Collaborate with cross-functional stakeholders, operating independently within a sponsor-dedicated environment.

🎯 Requirements

• Doctoral degree in Epidemiology • 5–7 years of experience within a pharma company or pharma consulting environment • Experience conducting real-world evidence studies using secondary data sources, including commercial RWD platforms (e.g., HealthVerity, PharMetrics Plus, TriNetX) • Strong understanding of regulatory requirements supporting clinical development, including the types of evidence required to address safety and evidence gaps for Phase 2 and Phase 3 programs • Experience supporting clinical development and/or drug safety through observational research • Ability to work with and interpret large healthcare datasets; advanced programming not required • Strong ability to collaborate across cross-functional teams and contribute to study design, execution, and interpretation

🏖️ Benefits

• Access IQVIA’s global network who supports your growth. • Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare. • Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies. • Opportunity to make an impact while building a career that matters.