Bristol-Myers Squibb
Scientific Associate Director - Toxicology
Bristol-Myers Squibb, New Brunswick, New Jersey, us, 08933
Scientific Associate Director - Toxicology
ApplyLocations:
New Brunswick - NJ - US, Brisbane - CA - US, Princeton - NJ - US, Cambridge Crossing - MA - US, San Diego - CA - USTime Type:
Full timePosted On:
Posted 30+ Days AgoJob Requisition ID:
R1584005Working with UsChallenging. 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 rich in diversity. 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.This is a Hybrid role.Position OverviewIn 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 exploratory and pivotal toxicity studies, including single- and repeat-dose toxicity, investigative toxicity, and other toxicity studies.Acts 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.Interacts with regulatory agencies worldwide on issues of nonclinical safety evaluation as needed.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 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:12+ years of academic/industry experienceOr Master's Degree with 10+ years of academic/industry experienceOR PhD with 8+ years of academic/industry experience and 4+ years of leadership experiencePreferred Qualifications:10+ years of regulatory toxicology/development experience.Knowledge of biochemical and mechanistic toxicology, immunology, pharmacology, biology of disease, and/or experimental pathology.Effective written and oral communication skills, especially as they pertain to writing clear, and accurate documents and presenting data.Ability to manage multiple research activities, provide and accept input on data interpretation, foster a spirit of team effort, and work well with others.Ability to interpret and apply available toxicity data to assess relative risk or hazard to humans.The starting compensation for this job is a range from $185,000 to $231,300, plus incentive cash and stock opportunities (based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. Final individual compensation will be decided based on demonstrated experience.Life At BMS - BMS Careers#LI-HybridIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing CareersWith a single vision as inspiring as 'Transforming patients’ lives through science', every BMS employee plays an integral role in work that goes far beyond ordinary.
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ApplyLocations:
New Brunswick - NJ - US, Brisbane - CA - US, Princeton - NJ - US, Cambridge Crossing - MA - US, San Diego - CA - USTime Type:
Full timePosted On:
Posted 30+ Days AgoJob Requisition ID:
R1584005Working with UsChallenging. 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 rich in diversity. 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.This is a Hybrid role.Position OverviewIn 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 exploratory and pivotal toxicity studies, including single- and repeat-dose toxicity, investigative toxicity, and other toxicity studies.Acts 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.Interacts with regulatory agencies worldwide on issues of nonclinical safety evaluation as needed.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 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:12+ years of academic/industry experienceOr Master's Degree with 10+ years of academic/industry experienceOR PhD with 8+ years of academic/industry experience and 4+ years of leadership experiencePreferred Qualifications:10+ years of regulatory toxicology/development experience.Knowledge of biochemical and mechanistic toxicology, immunology, pharmacology, biology of disease, and/or experimental pathology.Effective written and oral communication skills, especially as they pertain to writing clear, and accurate documents and presenting data.Ability to manage multiple research activities, provide and accept input on data interpretation, foster a spirit of team effort, and work well with others.Ability to interpret and apply available toxicity data to assess relative risk or hazard to humans.The starting compensation for this job is a range from $185,000 to $231,300, plus incentive cash and stock opportunities (based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. Final individual compensation will be decided based on demonstrated experience.Life At BMS - BMS Careers#LI-HybridIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing CareersWith a single vision as inspiring as 'Transforming patients’ lives through science', every BMS employee plays an integral role in work that goes far beyond ordinary.
#J-18808-Ljbffr