Associate Director, Clinical Pathologist

🕒 September 30

🇺🇸 United States – Remote

💵 $176.1k - $287.3k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Regeneron

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1988

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

💰 Post-IPO Equity on 2023-10

Healthcare • Manufacturing • Biotechnology

Regeneron is a biotechnology company dedicated to turning scientific discoveries into life-changing medicines. The company focuses on a range of serious diseases including allergic, cardiovascular, and metabolic diseases, neuroscience, oncology, hematology, ophthalmology, and rare diseases. It achieves this by integrating biology and technology to develop cutting-edge biologics and genetic medicines. Regeneron is committed to health equity, environmental sustainability, and supporting future STEM talent through initiatives like the Regeneron Science Talent Search. By maintaining high ethical standards and corporate responsibility, Regeneron aims to push the boundaries of science for better healthcare solutions.

📋 Description

• Serve as a scientific leader supporting nonclinical drug development across multiple therapeutic areas • Work independently and as part of integrated discovery and development teams • Interpret pharmacologic and toxicity-related findings to advance promising therapeutics through Regeneron’s pipeline • Determine and evaluate clinical pathology-related endpoints in pharmacology and toxicology studies • Guide decision-making based on clinical pathology findings • Collaborate with anatomic pathologists, toxicologists, and researchers within Regeneron • Partner with CROs to provide scientific peer review of nonclinical safety studies • Manage Clinical Pathology support for selected therapeutic focus areas • Mentor junior Pathologists • Support drug molecule efficacy and safety studies, including GLP toxicology and PK studies

🎯 Requirements

• DVM (or equivalent) with ACVP certification in Clinical Pathology required • Minimum 3 years of industry experience interpreting GLP and non-GLP clinical pathology data in nonclinical studies and supporting discovery research in a pharma/biotech or CRO setting • Experience integrating clinical and anatomic pathology data • Experience with animal models of human diseases • Clear, concise oral and written communication skills • Demonstrated ability to contribute to cross-functional teams • Ability to contribute to scientific strategy, problem solving, and broader understanding of pathology-related issues influencing drug development outcomes • Additional certification in Anatomic Pathology is nice to have • Background checks may be conducted, including verification of identity, right to work, and educational qualifications

🏖️ Benefits

• Annual bonuses or other incentive plans • Equity awards • Pension or retirement benefits • 401(k) company match • Health and wellness programs • Fitness centers • Medical, dental, vision, life and disability insurance benefits • Paid time off • Family support benefits • Reasonable accommodation during the recruitment process where required

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