Associate Manager, Toxicology Operations

Regeneron Pharmaceuticals, Inc (USA); United States; Hybrid; USD 120,000 - 180,000; Full time

Benefits offered by this job

Annual bonuses or incentive plans

Equity awards

Pension/retirement benefits

401(k) company match

Health and wellness programs

Fitness centers

Insurance benefits (medical, dental, 视

Paid time off

Family support benefits

Job summary

Regeneron Pharmaceuticals, Inc. in the United States is seeking an Associate Manager, Toxicology Operations to lead departmental operations and oversee study monitoring for outsourced toxicology studies.

The role supports GLP and non-GLP programs with limited supervision, coordinating logistics and maintaining SOPs. The candidate should have a strong background in toxicology study design, monitoring, and interpretation, and excellent communication skills to interact with cross-functional teams.

Qualifications

• Bachelor's degree in biological sciences; 6–8+ years post-degree experience; Master's preferred.
• Strong understanding of toxicologic investigation theory and rationale.
• Significant experience in design, monitoring, and interpretation of regulated nonclinical safety studies.
• Ability to communicate effectively with stakeholders at all levels of drug safety and pharmacometrics.

Responsibilities

• Lead operational role for the Toxicology department with limited supervision.
• Oversee completion of department goals and direct junior specialists.
• Collect and maintain metrics for toxicology studies (timelines, costs, etc.).
• Maintain department SOPs database and contribute to study design concepts.
• Coordinate all aspects of logistical support for outsourced studies (GLP and non-GLP).

Skills

Leadership

Operations management

Study monitoring

Communication

Education

Bachelor's degree in biological sciences

Master's degree preferred

Job description

Build Our Future Together At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases.

As an Associate Manager, Toxicology Operations you will be utilizing your broad foundation in drug development obtained through academic training and industry experience to perform scientific, technical, and operational tasks with limited supervision to support the Toxicology department. You will contribute to toxicology studies and/or program development through study monitoring of outsourced non-GLP and GLP studies through remote and onsite CRO monitoring and other activities as assigned by their supervisor.

When & Where This position is approved to be hired remotely in the United States; EST hours preferred. Can also sit on-site in Tarrytown, NY if desired.

Discover Your Role

• Serves in a lead operational role for the Toxicology department.
• Responsible for overseeing completion of assigned department goals/activities with minimal supervision and directs junior specialists in the completion of support activities.
• Assists and or is responsible for the collection and maintenance of metrics associated with the conduct of Toxicology studies (timelines, costs, etc.).
• Responsible for maintenance of department SOPs database.
• Capable of acting as lead study monitor on GLP toxicology studies and contributes to the development of study design concepts and protocols.
• Independently coordinates all aspects of logistical support for out-sourced studies.
• Develops protocols for outsourced toxicology studies with limited supervision.
• Independently conducts study monitoring remotely or on-site at CRO ensuring study conduct complies with approved protocols and amendments.
• Provides initial review and summation of Toxicology study data/reports and recommends areas for further evaluation by supervisor or senior Toxicology staff.
• Actively participates in department meetings providing input on operational strategies.

This Role Requires

• Minimum of a Bachelor's degree in biological sciences with 6-8+ years of post-degree experience within a pharmaceutical/drug development environment; Master's degree preferred.
• A well-developed understanding of the theory and rationale that underlie methods used in toxicologic investigations.
• Significant experience in the design, monitoring and interpretation of regulated nonclinical safety studies required.
• Capable of communicating at all levels of drug safety and pharmacometrics.

We are committed to building a workplace with an inclusive culture.

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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role:

• annual bonuses or other incentive plans
• equity awards
• pension or retirement benefits
• 401(k) company match
• health and wellness programs
• fitness centers
• insurance benefits (e.g. medical, dental, vision, life and disability)
• paid time off
• family support benefits

For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process.

Please be advised that at Regeneron, we believe we do our best work when we are together.

For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position. Salary Range (annually) $98,100.00 - $160,100.00

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA‑approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories.

Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases.

Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.