Scientific Associate Director - Toxicology
Bristol Myers Squibb, Seattle, WA, United States
Working with Us
Challenging. Meaningful. Life‑changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Position Overview In the role as a
Project Toxicologist , the ideal candidate:
Is responsible for the oversight of the nonclinical safety evaluation programs for selected drug candidates.
Assists in the proper design and timely reporting of toxicity studies (GLP/nonGLP), including single‑ and repeat‑dose toxicity, investigative toxicity, and other toxicity studies as required.
Act as a Nonclinical Safety representative on early‑ and late‑stage project development teams.
Provides scientifically and strategically sound nonclinical development plans to management and development teams.
On an as‑needed basis, interacts with regulatory agencies worldwide on issues of nonclinical safety evaluation.
Writes and critically reviews submission documents, such as CTD sections for INDs and NDAs, IBs, PIPs, briefing books to support clinical trials and drug registration globally.
Participates in discussions with internal development teams and/or regulatory agencies to address safety findings and provide safety assessments.
Evaluates, proposes, and applies new scientific methodology to enhance scientific excellence and/or productivity in Nonclinical Safety. Works collaboratively across disciplines to identify, characterize, and resolve target/compound based toxicities.
Represents BMS in external scientific and regulatory collaborations, committees and consortia.
Gains broad‑based exposure to the various functional areas within Nonclinical Safety with an opportunity to perform independent research as appropriate.
Collaborates with the Discovery organization to help evaluate toxicity of drug candidates.
Ensures compliance with Good Laboratory Practice, Standard Operating Procedures, and study protocols in conducting nonclinical studies, when applicable. Ensures compliance with all company/departmental policies, particularly those relating to animal welfare and safety.
Embraces/demonstrates BMS Core Values to create an atmosphere of scientific excellence, open communication, and creativity in order to maximize productivity.
Basic Qualifications
Bachelor's Degree and 15+ years of academic / industry experience
Master's Degree and 12+ years of academic / industry experience
PhD and 8+ years of academic / industry experience
Plus 6+ years of leadership experience
Preferred Qualifications
10+ years regulatory toxicology/development experience.
Knowledge of biochemical and mechanistic toxicology, immunology, pharmacology, biology of disease, and/or experimental pathology. Experience designing and interpreting in vitro and in vivo studies exploring mechanisms of toxicology involving biochemical, immunological, functional, molecular, and/or structural endpoints.
Effective written and oral communication skills, especially as they pertain to writing clear, and accurate documents and presenting data.
Individual must be able to manage multiple research activities, provide and accept input on data interpretation, foster a spirit of team effort, and be able to work well with others.
Ability to interpret and apply available toxicity data to assess relative risk or hazard to humans.
Compensation Overview
Brisbane - CA - US: $205,490 - $249,003
Cambridge Crossing: $205,490 - $249,003
New Brunswick - NJ - US: $178,690 - $216,527
Princeton - NJ - US: $178,690 - $216,527
San Diego - CA - US: $196,550 - $238,177
Seattle - WA: $196,550 - $238,177
The starting compensation range(s) for this role are listed above for a full‑time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job‑related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefits
Health Coverage:
Medical, pharmacy, dental and vision care.
Well‑Being Support:
Programs such as BMS Well‑Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well‑Being and Protection:
401(k) plan, short‑ and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support and survivor support.
Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Equal Employment Opportunity Statement Bristol Myers Squibb is an equal‑opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation or any other characteristic protected by law.
Req Number: R1597887
Updated: 2026‑04‑03 02:09:36.634 UTC
#J-18808-Ljbffr
Challenging. Meaningful. Life‑changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Position Overview In the role as a
Project Toxicologist , the ideal candidate:
Is responsible for the oversight of the nonclinical safety evaluation programs for selected drug candidates.
Assists in the proper design and timely reporting of toxicity studies (GLP/nonGLP), including single‑ and repeat‑dose toxicity, investigative toxicity, and other toxicity studies as required.
Act as a Nonclinical Safety representative on early‑ and late‑stage project development teams.
Provides scientifically and strategically sound nonclinical development plans to management and development teams.
On an as‑needed basis, interacts with regulatory agencies worldwide on issues of nonclinical safety evaluation.
Writes and critically reviews submission documents, such as CTD sections for INDs and NDAs, IBs, PIPs, briefing books to support clinical trials and drug registration globally.
Participates in discussions with internal development teams and/or regulatory agencies to address safety findings and provide safety assessments.
Evaluates, proposes, and applies new scientific methodology to enhance scientific excellence and/or productivity in Nonclinical Safety. Works collaboratively across disciplines to identify, characterize, and resolve target/compound based toxicities.
Represents BMS in external scientific and regulatory collaborations, committees and consortia.
Gains broad‑based exposure to the various functional areas within Nonclinical Safety with an opportunity to perform independent research as appropriate.
Collaborates with the Discovery organization to help evaluate toxicity of drug candidates.
Ensures compliance with Good Laboratory Practice, Standard Operating Procedures, and study protocols in conducting nonclinical studies, when applicable. Ensures compliance with all company/departmental policies, particularly those relating to animal welfare and safety.
Embraces/demonstrates BMS Core Values to create an atmosphere of scientific excellence, open communication, and creativity in order to maximize productivity.
Basic Qualifications
Bachelor's Degree and 15+ years of academic / industry experience
Master's Degree and 12+ years of academic / industry experience
PhD and 8+ years of academic / industry experience
Plus 6+ years of leadership experience
Preferred Qualifications
10+ years regulatory toxicology/development experience.
Knowledge of biochemical and mechanistic toxicology, immunology, pharmacology, biology of disease, and/or experimental pathology. Experience designing and interpreting in vitro and in vivo studies exploring mechanisms of toxicology involving biochemical, immunological, functional, molecular, and/or structural endpoints.
Effective written and oral communication skills, especially as they pertain to writing clear, and accurate documents and presenting data.
Individual must be able to manage multiple research activities, provide and accept input on data interpretation, foster a spirit of team effort, and be able to work well with others.
Ability to interpret and apply available toxicity data to assess relative risk or hazard to humans.
Compensation Overview
Brisbane - CA - US: $205,490 - $249,003
Cambridge Crossing: $205,490 - $249,003
New Brunswick - NJ - US: $178,690 - $216,527
Princeton - NJ - US: $178,690 - $216,527
San Diego - CA - US: $196,550 - $238,177
Seattle - WA: $196,550 - $238,177
The starting compensation range(s) for this role are listed above for a full‑time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job‑related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefits
Health Coverage:
Medical, pharmacy, dental and vision care.
Well‑Being Support:
Programs such as BMS Well‑Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well‑Being and Protection:
401(k) plan, short‑ and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support and survivor support.
Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Equal Employment Opportunity Statement Bristol Myers Squibb is an equal‑opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation or any other characteristic protected by law.
Req Number: R1597887
Updated: 2026‑04‑03 02:09:36.634 UTC
#J-18808-Ljbffr