We are looking for a Toxicologic Pathologist with extensive experience in the assessment of tissues from toxicology studies of large molecules. This Associate Director role will report directly to the Head of Pathology. The selected individual will have primary responsibility for pathology peer review of regulatory studies conducted at CROs. In addition, s/he will also provide pathology support of our in-house Discovery efforts across all Therapeutic Areas. S/he will also be encouraged to develop expertise in Ocular pathology, supporting Regeneron's growing portfolio of therapeutic molecules targeted at Ophthalmic indications.
A TYPICAL DAY MIGHT LOOK LIKE :
- Participate in strategy development in Drug Safety and Pharmacometrics (DSP) through advocacy for REGN programs and projects.
- Responsible for pathologic evaluation of drugs in a variety of therapeutic areas: Inflammation and Immunity, Pain, Oncology, Infectious Diseases, Skeletal and Muscle, Ophthalmology, Metabolic, Cardiac and Genetic Diseases collaborating with R&D, Regulatory and Clinical scientists to facilitate the actualization of Regeneron's Strategic Plan.
- Help design, develop, and implement research programs to support all facets of drug development.
- Perform pathology peer review of REGN toxicology studies at CROs (and therefore must be GLP-trained).
- Participate on teams devoted to developing predictive and prognostic biomarkers in assigned therapeutic areas.
- Collaborate to develop a strong in-house digital pathology program
- Deliver occasional seminars based on histopathologic data from assigned regulatory and discovery studies.
This position requires a DVM degree or foreign equivalent and Board Certification in Veterinary Pathology (Diplomate, ACVP or equivalent). The ideal candidate will also possess a PhD and/or other graduate degrees in Comparative Pathology or related field. The ability to interpret traditional diagnostic categories in the context of a detailed and current understanding of classical histopathology and molecular pathology is required. To that end, at least 6 years of toxicologic pathology experience (which may include the three years of residency training in Pathology). Additional requirements below:
- Clear demonstration of high-quality scholarly productivity in investigative pathology or other areas of biomedical research evidenced by publications is desirable.
- Demonstrated ability to handle regulatory as well as discovery projects and work successfully in a variety of therapeutic projects teams is desirable
- Experience with large molecule projects will be an advantage.
- The successful candidate will be familiar with, if not expert in molecular pathology and image analysis techniques
- Excellent verbal and written communication skills.
Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!
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 maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.