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Associate Director, Clinical Pharmacology and Pharmacometrics

Bristol-Myers Squibb

Healthcare Jobs

Associate Director, Clinical Pharmacology and Pharmacometrics

full-timePosted: Oct 27, 2025

Job Description

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. Read more: careers.bms.com/working-with-us. Summary The Clinical Pharmacology and Pharmacometrics (CP&P) team at BMS is responsible for the pharmacology and pharmacometric support for all pipeline assets throughout the clinical development lifecycle. Composed of pharmacologists, pharmacometricians, data scientists and modelers, this group oversees the pharmacokinetic evaluation, pharmacometric exposure-response evaluation, quantitative systems pharmacology modeling, physiologically based pharmacokinetic modeling and model based meta-analysis of assets covering all therapeutic modalities, including small molecules, traditional and complex biologics and next gen cell therapies. All therapeutic areas are supported. The CP&P team interacts with discovery and translational scientists, project leadership, early and late clinical development teams and commercial colleagues to provide input on clinical pharmacology profiling, dose optimization, formulation bridging, and combination strategies to enable faster and more effective drug development informed by core scientific principals and data. We are seeking a prospective candidate in our Lawrenceville, New Jersey office location. Responsibilities Independently contribute to compound development across various development phases Represent Clin Pharm on asset teams and at governance meetings based on proficiency Provide input to Phase 2/3 clinical study design and registrational strategy Accountable for the Clinical Pharmacology Plan Lead design of clinical pharmacology studies and manages data analysis, interpretation, and reporting High proficiency in PK, PK/PD, and model informed drug development (MIDD) principles and analyses Collaborate on cross-functional drug development teams, and regulatory submissions; serves as Clinical Pharmacology subject matter expert Requirements Advanced Degree in related field (MS, Ph.D. or PharmD) For Associate Director with Ph.D. approximately 5+ years of experience with demonstrated progression in clinical pharmacology and pharmacometrics. For M.S. Degree, 10 years of experience with demonstrated progression in clinical pharmacology and pharmacometrics Demonstrated ability to work in a dynamic team-oriented environment Experience leading a Clinical Pharmacology team is required for the Director level position. Expertise in general drug development Expertise in small molecule and/or biologic drug property characterization Demonstrated stakeholder management with strong influence/leadership Hands on and demonstrated Pharmacometrics experience required including exposure-response modeling Quantitative data analysis, POP PK/PD, and data visualization skills Programming experience (e.g., NONMEN, Phoenix NLME, Monolix, R, WinNonlin, SAS, Splus etc.) Ability to work hybrid work hours in office 50% of the time per week located in Princeton BMS office LI-HYBRID If 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. Compensation Overview: Princeton - NJ - US: $181,960 - $220,492 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/. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program. Uniquely Interesting Work, Life-changing Careers With 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. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

About the Role/Company

  • Bristol Myers Squibb is a company where challenging, meaningful, and life-changing work happens every day
  • The Clinical Pharmacology and Pharmacometrics (CP&P) team at BMS is responsible for the pharmacology and pharmacometric support for all pipeline assets throughout the clinical development lifecycle
  • The CP&P team is composed of pharmacologists, pharmacometricians, data scientists, and modelers
  • The team oversees pharmacokinetic evaluation, pharmacometric exposure-response evaluation, quantitative systems pharmacology modeling, physiologically based pharmacokinetic modeling, and model-based meta-analysis of assets covering all therapeutic modalities
  • The CP&P team interacts with discovery and translational scientists, project leadership, early and late clinical development teams, and commercial colleagues to provide input on clinical pharmacology profiling, dose optimization, formulation bridging, and combination strategies
  • BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments, and ongoing support in their roles
  • BMS strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters
  • BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area

Key Responsibilities

  • Independently contribute to compound development across various development phases
  • Represent Clin Pharm on asset teams and at governance meetings based on proficiency
  • Provide input to Phase 2/3 clinical study design and registrational strategy
  • Accountable for the Clinical Pharmacology Plan
  • Lead design of clinical pharmacology studies and manage data analysis, interpretation, and reporting
  • High proficiency in PK, PK/PD, and model informed drug development (MIDD) principles and analyses
  • Collaborate on cross-functional drug development teams, and regulatory submissions; serve as Clinical Pharmacology subject matter expert

Required Qualifications

  • Advanced Degree in related field (MS, Ph.D., or PharmD)
  • For Associate Director with Ph.D., approximately 5+ years of experience with demonstrated progression in clinical pharmacology and pharmacometrics
  • For M.S. Degree, 10 years of experience with demonstrated progression in clinical pharmacology and pharmacometrics
  • Experience leading a Clinical Pharmacology team is required for the Director level position

Skills Required

  • Expertise in general drug development
  • Expertise in small molecule and/or biologic drug property characterization
  • Demonstrated stakeholder management with strong influence/leadership
  • Hands on and demonstrated Pharmacometrics experience required including exposure-response modeling
  • Quantitative data analysis, POP PK/PD, and data visualization skills
  • Programming experience (e.g., NONMEN, Phoenix NLME, Monolix, R, WinNonlin, SAS, Splus etc.)

Benefits & Perks

  • Competitive benefits, services, and programs
  • Medical, pharmacy, dental, and vision care
  • Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
  • Financial well-being resources and a 401(K)
  • Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support
  • Work-life programs including paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility
  • Parental, caregiver, bereavement, and military leave
  • Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources
  • Other perks like tuition reimbursement and a recognition program

Additional Requirements

  • Ability to work hybrid work hours in office 50% of the time per week located in Princeton BMS office

Locations

  • Princeton NJ, United States

Salary

181,960 - 220,492 USD / yearly

Skills Required

  • Expertise in general drug developmentintermediate
  • Expertise in small molecule and/or biologic drug property characterizationintermediate
  • Demonstrated stakeholder management with strong influence/leadershipintermediate
  • Hands on and demonstrated Pharmacometrics experience required including exposure-response modelingintermediate
  • Quantitative data analysis, POP PK/PD, and data visualization skillsintermediate
  • Programming experience (e.g., NONMEN, Phoenix NLME, Monolix, R, WinNonlin, SAS, Splus etc.)intermediate

Required Qualifications

  • Advanced Degree in related field (MS, Ph.D., or PharmD) (experience)
  • For Associate Director with Ph.D., approximately 5+ years of experience with demonstrated progression in clinical pharmacology and pharmacometrics (experience)
  • For M.S. Degree, 10 years of experience with demonstrated progression in clinical pharmacology and pharmacometrics (experience)
  • Experience leading a Clinical Pharmacology team is required for the Director level position (experience)

Responsibilities

  • Independently contribute to compound development across various development phases
  • Represent Clin Pharm on asset teams and at governance meetings based on proficiency
  • Provide input to Phase 2/3 clinical study design and registrational strategy
  • Accountable for the Clinical Pharmacology Plan
  • Lead design of clinical pharmacology studies and manage data analysis, interpretation, and reporting
  • High proficiency in PK, PK/PD, and model informed drug development (MIDD) principles and analyses
  • Collaborate on cross-functional drug development teams, and regulatory submissions; serve as Clinical Pharmacology subject matter expert

Benefits

  • general: Competitive benefits, services, and programs
  • general: Medical, pharmacy, dental, and vision care
  • general: Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
  • general: Financial well-being resources and a 401(K)
  • general: Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support
  • general: Work-life programs including paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility
  • general: Parental, caregiver, bereavement, and military leave
  • general: Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources
  • general: Other perks like tuition reimbursement and a recognition program

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Bristol-Myers Squibb logo

Associate Director, Clinical Pharmacology and Pharmacometrics

Bristol-Myers Squibb

Healthcare Jobs

Associate Director, Clinical Pharmacology and Pharmacometrics

full-timePosted: Oct 27, 2025

Job Description

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. Read more: careers.bms.com/working-with-us. Summary The Clinical Pharmacology and Pharmacometrics (CP&P) team at BMS is responsible for the pharmacology and pharmacometric support for all pipeline assets throughout the clinical development lifecycle. Composed of pharmacologists, pharmacometricians, data scientists and modelers, this group oversees the pharmacokinetic evaluation, pharmacometric exposure-response evaluation, quantitative systems pharmacology modeling, physiologically based pharmacokinetic modeling and model based meta-analysis of assets covering all therapeutic modalities, including small molecules, traditional and complex biologics and next gen cell therapies. All therapeutic areas are supported. The CP&P team interacts with discovery and translational scientists, project leadership, early and late clinical development teams and commercial colleagues to provide input on clinical pharmacology profiling, dose optimization, formulation bridging, and combination strategies to enable faster and more effective drug development informed by core scientific principals and data. We are seeking a prospective candidate in our Lawrenceville, New Jersey office location. Responsibilities Independently contribute to compound development across various development phases Represent Clin Pharm on asset teams and at governance meetings based on proficiency Provide input to Phase 2/3 clinical study design and registrational strategy Accountable for the Clinical Pharmacology Plan Lead design of clinical pharmacology studies and manages data analysis, interpretation, and reporting High proficiency in PK, PK/PD, and model informed drug development (MIDD) principles and analyses Collaborate on cross-functional drug development teams, and regulatory submissions; serves as Clinical Pharmacology subject matter expert Requirements Advanced Degree in related field (MS, Ph.D. or PharmD) For Associate Director with Ph.D. approximately 5+ years of experience with demonstrated progression in clinical pharmacology and pharmacometrics. For M.S. Degree, 10 years of experience with demonstrated progression in clinical pharmacology and pharmacometrics Demonstrated ability to work in a dynamic team-oriented environment Experience leading a Clinical Pharmacology team is required for the Director level position. Expertise in general drug development Expertise in small molecule and/or biologic drug property characterization Demonstrated stakeholder management with strong influence/leadership Hands on and demonstrated Pharmacometrics experience required including exposure-response modeling Quantitative data analysis, POP PK/PD, and data visualization skills Programming experience (e.g., NONMEN, Phoenix NLME, Monolix, R, WinNonlin, SAS, Splus etc.) Ability to work hybrid work hours in office 50% of the time per week located in Princeton BMS office LI-HYBRID If 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. Compensation Overview: Princeton - NJ - US: $181,960 - $220,492 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/. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program. Uniquely Interesting Work, Life-changing Careers With 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. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

About the Role/Company

  • Bristol Myers Squibb is a company where challenging, meaningful, and life-changing work happens every day
  • The Clinical Pharmacology and Pharmacometrics (CP&P) team at BMS is responsible for the pharmacology and pharmacometric support for all pipeline assets throughout the clinical development lifecycle
  • The CP&P team is composed of pharmacologists, pharmacometricians, data scientists, and modelers
  • The team oversees pharmacokinetic evaluation, pharmacometric exposure-response evaluation, quantitative systems pharmacology modeling, physiologically based pharmacokinetic modeling, and model-based meta-analysis of assets covering all therapeutic modalities
  • The CP&P team interacts with discovery and translational scientists, project leadership, early and late clinical development teams, and commercial colleagues to provide input on clinical pharmacology profiling, dose optimization, formulation bridging, and combination strategies
  • BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments, and ongoing support in their roles
  • BMS strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters
  • BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area

Key Responsibilities

  • Independently contribute to compound development across various development phases
  • Represent Clin Pharm on asset teams and at governance meetings based on proficiency
  • Provide input to Phase 2/3 clinical study design and registrational strategy
  • Accountable for the Clinical Pharmacology Plan
  • Lead design of clinical pharmacology studies and manage data analysis, interpretation, and reporting
  • High proficiency in PK, PK/PD, and model informed drug development (MIDD) principles and analyses
  • Collaborate on cross-functional drug development teams, and regulatory submissions; serve as Clinical Pharmacology subject matter expert

Required Qualifications

  • Advanced Degree in related field (MS, Ph.D., or PharmD)
  • For Associate Director with Ph.D., approximately 5+ years of experience with demonstrated progression in clinical pharmacology and pharmacometrics
  • For M.S. Degree, 10 years of experience with demonstrated progression in clinical pharmacology and pharmacometrics
  • Experience leading a Clinical Pharmacology team is required for the Director level position

Skills Required

  • Expertise in general drug development
  • Expertise in small molecule and/or biologic drug property characterization
  • Demonstrated stakeholder management with strong influence/leadership
  • Hands on and demonstrated Pharmacometrics experience required including exposure-response modeling
  • Quantitative data analysis, POP PK/PD, and data visualization skills
  • Programming experience (e.g., NONMEN, Phoenix NLME, Monolix, R, WinNonlin, SAS, Splus etc.)

Benefits & Perks

  • Competitive benefits, services, and programs
  • Medical, pharmacy, dental, and vision care
  • Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
  • Financial well-being resources and a 401(K)
  • Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support
  • Work-life programs including paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility
  • Parental, caregiver, bereavement, and military leave
  • Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources
  • Other perks like tuition reimbursement and a recognition program

Additional Requirements

  • Ability to work hybrid work hours in office 50% of the time per week located in Princeton BMS office

Locations

  • Princeton NJ, United States

Salary

181,960 - 220,492 USD / yearly

Skills Required

  • Expertise in general drug developmentintermediate
  • Expertise in small molecule and/or biologic drug property characterizationintermediate
  • Demonstrated stakeholder management with strong influence/leadershipintermediate
  • Hands on and demonstrated Pharmacometrics experience required including exposure-response modelingintermediate
  • Quantitative data analysis, POP PK/PD, and data visualization skillsintermediate
  • Programming experience (e.g., NONMEN, Phoenix NLME, Monolix, R, WinNonlin, SAS, Splus etc.)intermediate

Required Qualifications

  • Advanced Degree in related field (MS, Ph.D., or PharmD) (experience)
  • For Associate Director with Ph.D., approximately 5+ years of experience with demonstrated progression in clinical pharmacology and pharmacometrics (experience)
  • For M.S. Degree, 10 years of experience with demonstrated progression in clinical pharmacology and pharmacometrics (experience)
  • Experience leading a Clinical Pharmacology team is required for the Director level position (experience)

Responsibilities

  • Independently contribute to compound development across various development phases
  • Represent Clin Pharm on asset teams and at governance meetings based on proficiency
  • Provide input to Phase 2/3 clinical study design and registrational strategy
  • Accountable for the Clinical Pharmacology Plan
  • Lead design of clinical pharmacology studies and manage data analysis, interpretation, and reporting
  • High proficiency in PK, PK/PD, and model informed drug development (MIDD) principles and analyses
  • Collaborate on cross-functional drug development teams, and regulatory submissions; serve as Clinical Pharmacology subject matter expert

Benefits

  • general: Competitive benefits, services, and programs
  • general: Medical, pharmacy, dental, and vision care
  • general: Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
  • general: Financial well-being resources and a 401(K)
  • general: Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support
  • general: Work-life programs including paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility
  • general: Parental, caregiver, bereavement, and military leave
  • general: Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources
  • general: Other perks like tuition reimbursement and a recognition program

Target Your Resume for "Associate Director, Clinical Pharmacology and Pharmacometrics" , Bristol-Myers Squibb

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ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
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Tags & Categories

PharmaceuticalPharmaceuticalHealthcare

Answer 10 quick questions to check your fit for Associate Director, Clinical Pharmacology and Pharmacometrics @ Bristol-Myers Squibb.

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~2 Minutes
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