Manager - Toxicology Operations - Remote

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Toxicology Operations Manager to join our Toxicology team, leading scientific, technical, and operational tasks as assigned to support toxicology program representatives and toxicology department leadership. In this role, you will independently manage and be responsible for the contracting, drug supply, protocol development, and conduct of non-GLP and GLP Toxicology studies through remote and on-site CRO monitoring.

The individual will also contribute to the review and evaluation of study data providing program toxicologists with data summaries to enable alignment on study results. The individual will also contribute outside of the Toxicology department presenting study results to preclinical subteams and global project teams as required.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

Location – Full Time - Remote position with occasional International and Domestic travel.

• Serves in a principal operational role for the Toxicology department, ensuring assigned department and project goals are achieved as assigned
• Assists in defining standard departmental practices (including SOPs) for the conduct and reporting of Toxicology studies
• Serves as the lead study monitor or sponsor representative with administrative oversight related to the conduct of Toxicology studies conducted at CRO
• Collaborates with lead scientists providing direct input and suggestions on study designs and protocols
• Responsible for independent coordination of study outsourcing (RFP, contracting, protocol development, monitoring, and reporting)
• Provides detailed evaluation of experimental data from Toxicology studies and aligns with program toxicologists to interpret, report and present results
• Assists/Directs the collection and evaluation of metrics associated with the conduct of Toxicology studies
• Provides toxicology leadership assistance in regulatory inspection readiness activities

• Bachelor’s or Master’s degree in biological sciences with more than 7 years of post‑degree experience within a pharmaceutical/drug development environment.
• Significant experience in the design, monitoring and interpretation of regulated nonclinical safety studies.
• Knowledge of communicating Toxicology study results up to the level of global project teams.
• Ability to trouble‑shoot challenges arising during the conduct of Toxicology studies

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!

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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.