Associate Director, Clinical Pathologist

Regeneron Pharmaceuticals, Inc.; Village of Tarrytown (NY); On-site; USD 176,100 - 287,300; Full time

Benefits offered by this job

Health and wellness programs

401(k) company match

Annual bonuses

Paid time off

Job summary

Regeneron is seeking an Associate Director of Pathology in Tarrytown, NY, to support drug efficacy and safety studies. You will lead clinical pathology initiatives, mentor junior pathologists, and collaborate with multifaceted teams to advance therapeutics.

Ideal candidates will have a DVM with ACVP certification and at least three years of relevant experience. The role offers comprehensive benefits including health programs, 401(k) match, annual bonuses, and paid time off. Join us in making a difference!

Qualifications

• Minimum 3 years of experience interpreting GLP and non-GLP clinical pathology data.
• Supporting discovery research in pharma/biotech or CRO.

Responsibilities

• Serve as a scientific leader supporting nonclinical drug development.
• Work independently and collaboratively to interpret findings.
• Determine and evaluate clinical pathology related endpoints.
• Collaborate closely with anatomic pathologists and toxicologists.
• Partner with CROs for scientific peer review.

Skills

Integrating clinical and anatomic pathology data

Experience with animal models of human diseases

Clear communication skills

Team collaboration

Scientific strategy contribution

Education

DVM (or equivalent) with ACVP certification in Clinical Pathology

PhD preferred

Certification in Anatomic Pathology

Job description

Associate Director of Pathology has primary responsibility to support drug molecule efficacy and safety studies in a variety of therapeutic focus areas (TFAs). The successful candidate will also provide Clinical Pathology support for GLP toxicology and PK studies of Regeneron molecules. The Associate Director will be expected to manage Clinical Pathology support to selected TFAs, and mentor junior Pathologists.

A Typical Day In This Role May Look Like

• Serve as a scientific leader supporting nonclinical drug development across multiple therapeutic areas.
• Work both independently and as a part of integrated discovery and development teams to interpret pharmacologic and toxicity related findings and help advance promising therapeutics through Regeneron’s pipeline.
• Determining and evaluating clinical pathology related endpoints in pharmacology and toxicology studies and guiding decision making.
• Collaborate closely with anatomic pathologists, toxicologists, and researchers within Regeneron.
• Partner with our CRO partners in providing scientific peer review of nonclinical safety studies.

This Job Might Be For You If You

• Experience with 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.
• Contributing to scientific strategy, problem solving, and the broader understanding of pathology-related issues that influence drug development outcomes.

In order to be considered for this role, you must have

• DVM (or equivalent) with ACVP certification in Clinical Pathology (strong preference for PhD).
• Minimum 3 years of experience interpreting GLP and non GLP clinical pathology data in nonclinical studies and supporting discovery research in pharma/ biotech or CRO.
• Certification in Anatomic Pathology.

We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels.

For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Salary Range (annually)

$176,100.00 - $287,300.00