Principal Toxicologist

We are looking for a Principal Toxicologist in the Drug Safety and Pharmacometrics group. This person utilizes her/his scientific background to lead nonclinical development programs with minimal direction. The person in this role is expected to have a deep understanding of global regulatory guidelines. They will ensure all aspects of nonclinical safety are met enabling progression of assigned programs at all stages of clinical development. We expect that this person will also lead multiple programs, demonstrating the ability to prioritize and meet timelines with high quality results. The Principal Toxicologist will demonstrate leadership, project influence and provide strategic direction on applicable programs.

A DAY IN THE LIFE OF A PRINCIPAL TOXICOLOGIST MAY INVOLVE:
- Act as toxicology lead on research and development project teams setting non-clinical safety assessment strategy

- Assist management in developing regulatory risk assessment strategies, program budgets, and timing of toxicology studies in relation to regulatory and clinical milestones.

- Work in collaboration with subject matter experts across the organization as needed to design and execute toxicology development programs in support of clinical development.

- Interacting with contract research organizations to coordinate, design, supervise, and report toxicology and safety pharmacology studies

- Effectively communicate toxicology findings to project teams, senior management and regulators.

- Prepare, review and edit toxicology sections of regulatory documents and participate in meetings with regulatory agencies as the need arises.

- Maintain currency with GLP regulations and ICH, FDA and EMEA non-clinical safety guidelines.

- Evaluate, select and monitor toxicology studies at various domestic and international

THIS MAY BE THE ROLE FOR YOU IF:
- You enjoy both internal and external collaboration

- You want to both drive internal process optimization and mentor and/or supervise junior toxicology staff.

- You keep up with the latest scientific developments by reading the current literature and attending conferences.

EXPERIENCE
This position requires a minimum of a Ph.D. + ≥ 5 years, or Master's Degree in pharmacology, toxicology or closely related biological science, and ≥ 15 years, working in toxicology/safety assessment, drug development, or contract research organization. Board Certification in Toxicology desirable.

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.