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Bristol-Myers Squibb logo

Director, MEG Lead Immunology & Neuroscience, Medical Evidence Generation

Bristol-Myers Squibb

Director, MEG Lead Immunology & Neuroscience, Medical Evidence Generation

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: December 2, 2025

Number of Vacancies: 1

Job Description

Responsibilities will include, but are not limited to, the following: Facilitate collaborative exchange between BMS and thought leaders in community practice and academia, including scientific dialogue and representing BMS as a trusted, inclusive, and innovative industry collaborator and partner of choice. Provide oversight of Medical clinical trials end-to-end (i.e., start-up, influence governance outcomes, partner with contract Manager/Lead for agreement initiation, negotiation, execution, oversight throughout study and support readout) Design and drive strategies to accelerate the development of BMS's clinical development pipeline leveraging external research platforms, technologies, and insights. Contribute to the evolution of MEG therapeutic area strategy and value proposition. 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. Supporting People with Disabilities Advanced scientific degree (MD, PhD, PharmD, MS or the equivalent) required with extensive, relevant scientific, and/or clinical experience. At least 5 years of experience in pharmaceutical clinical development, Medical Affairs, or relevant Commercial experience; previous customer-facing role experience highly desirable. Demonstrated ability to strategically analyze data generation opportunities with minimal supervision. Demonstrated ability to develop and sustain high-performing relationships with external thought leaders and internal matrix stakeholders. Adeptness at building credibility with external investigators and collaborative partners competently balancing business and scientific acumen complemented by strong leadership behaviors, authenticity, agility, and an enterprise mindset. Understanding of global healthcare systems and academic settings with a demonstrated ability to lead in ambiguous and changing healthcare/business environments Exceptional communication and interpersonal skills to influence decision-making at all levels of the organization. In depth knowledge of overall project planning and project management of clinical trials Proven ability to partner effectively with colleagues across multiple functions and at all levels of the enterprise. Exceptional interpersonal and communication skills appropriately flexing based on audience; expertly leverages effective communication and negotiation skills to influence decisions. Expected 20%-30% travel globally.

About the Role/Company

  • BMS is a trusted, inclusive, and innovative industry collaborator and partner of choice

Key Responsibilities

  • Facilitate collaborative exchange between BMS and thought leaders in community practice and academia
  • Provide oversight of Medical clinical trials end-to-end including start-up, governance outcomes, contract management, execution, and study support
  • Design and drive strategies to accelerate the development of BMS's clinical development pipeline
  • Leverage external research platforms, technologies, and insights
  • Contribute to the evolution of MEG therapeutic area strategy and value proposition

Required Qualifications

  • Advanced scientific degree (MD, PhD, PharmD, MS or the equivalent) required
  • At least 5 years of experience in pharmaceutical clinical development, Medical Affairs, or relevant Commercial experience

Preferred Qualifications

  • Previous customer-facing role experience highly desirable

Skills Required

  • Demonstrated ability to strategically analyze data generation opportunities with minimal supervision
  • Ability to develop and sustain high-performing relationships with external thought leaders and internal matrix stakeholders
  • Adeptness at building credibility with external investigators and collaborative partners
  • Competent balance of business and scientific acumen
  • Strong leadership behaviors, authenticity, agility, and an enterprise mindset
  • Understanding of global healthcare systems and academic settings
  • Ability to lead in ambiguous and changing healthcare/business environments
  • Exceptional communication and interpersonal skills to influence decision-making at all levels of the organization
  • In-depth knowledge of overall project planning and project management of clinical trials
  • Proven ability to partner effectively with colleagues across multiple functions and at all levels of the enterprise
  • Expertly leverage effective communication and negotiation skills to influence decisions

Benefits & Perks

  • 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
  • Summer hours flexibility
  • Support for people with disabilities

Additional Requirements

  • Expected 20%-30% travel globally

Locations

  • Princeton NJ, United States
  • Madison Giralda NJ, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

250,000 - 350,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Demonstrated ability to strategically analyze data generation opportunities with minimal supervisionintermediate
  • Ability to develop and sustain high-performing relationships with external thought leaders and internal matrix stakeholdersintermediate
  • Adeptness at building credibility with external investigators and collaborative partnersintermediate
  • Competent balance of business and scientific acumenintermediate
  • Strong leadership behaviors, authenticity, agility, and an enterprise mindsetintermediate
  • Understanding of global healthcare systems and academic settingsintermediate
  • Ability to lead in ambiguous and changing healthcare/business environmentsintermediate
  • Exceptional communication and interpersonal skills to influence decision-making at all levels of the organizationintermediate
  • In-depth knowledge of overall project planning and project management of clinical trialsintermediate
  • Proven ability to partner effectively with colleagues across multiple functions and at all levels of the enterpriseintermediate
  • Expertly leverage effective communication and negotiation skills to influence decisionsintermediate

Required Qualifications

  • Advanced scientific degree (MD, PhD, PharmD, MS or the equivalent) required (experience)
  • At least 5 years of experience in pharmaceutical clinical development, Medical Affairs, or relevant Commercial experience (experience)

Preferred Qualifications

  • Previous customer-facing role experience highly desirable (experience)

Responsibilities

  • Facilitate collaborative exchange between BMS and thought leaders in community practice and academia
  • Provide oversight of Medical clinical trials end-to-end including start-up, governance outcomes, contract management, execution, and study support
  • Design and drive strategies to accelerate the development of BMS's clinical development pipeline
  • Leverage external research platforms, technologies, and insights
  • Contribute to the evolution of MEG therapeutic area strategy and value proposition

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility
  • general: Support for people with disabilities

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Bristol-Myers Squibb logo

Director, MEG Lead Immunology & Neuroscience, Medical Evidence Generation

Bristol-Myers Squibb

Director, MEG Lead Immunology & Neuroscience, Medical Evidence Generation

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: December 2, 2025

Number of Vacancies: 1

Job Description

Responsibilities will include, but are not limited to, the following: Facilitate collaborative exchange between BMS and thought leaders in community practice and academia, including scientific dialogue and representing BMS as a trusted, inclusive, and innovative industry collaborator and partner of choice. Provide oversight of Medical clinical trials end-to-end (i.e., start-up, influence governance outcomes, partner with contract Manager/Lead for agreement initiation, negotiation, execution, oversight throughout study and support readout) Design and drive strategies to accelerate the development of BMS's clinical development pipeline leveraging external research platforms, technologies, and insights. Contribute to the evolution of MEG therapeutic area strategy and value proposition. 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. Supporting People with Disabilities Advanced scientific degree (MD, PhD, PharmD, MS or the equivalent) required with extensive, relevant scientific, and/or clinical experience. At least 5 years of experience in pharmaceutical clinical development, Medical Affairs, or relevant Commercial experience; previous customer-facing role experience highly desirable. Demonstrated ability to strategically analyze data generation opportunities with minimal supervision. Demonstrated ability to develop and sustain high-performing relationships with external thought leaders and internal matrix stakeholders. Adeptness at building credibility with external investigators and collaborative partners competently balancing business and scientific acumen complemented by strong leadership behaviors, authenticity, agility, and an enterprise mindset. Understanding of global healthcare systems and academic settings with a demonstrated ability to lead in ambiguous and changing healthcare/business environments Exceptional communication and interpersonal skills to influence decision-making at all levels of the organization. In depth knowledge of overall project planning and project management of clinical trials Proven ability to partner effectively with colleagues across multiple functions and at all levels of the enterprise. Exceptional interpersonal and communication skills appropriately flexing based on audience; expertly leverages effective communication and negotiation skills to influence decisions. Expected 20%-30% travel globally.

About the Role/Company

  • BMS is a trusted, inclusive, and innovative industry collaborator and partner of choice

Key Responsibilities

  • Facilitate collaborative exchange between BMS and thought leaders in community practice and academia
  • Provide oversight of Medical clinical trials end-to-end including start-up, governance outcomes, contract management, execution, and study support
  • Design and drive strategies to accelerate the development of BMS's clinical development pipeline
  • Leverage external research platforms, technologies, and insights
  • Contribute to the evolution of MEG therapeutic area strategy and value proposition

Required Qualifications

  • Advanced scientific degree (MD, PhD, PharmD, MS or the equivalent) required
  • At least 5 years of experience in pharmaceutical clinical development, Medical Affairs, or relevant Commercial experience

Preferred Qualifications

  • Previous customer-facing role experience highly desirable

Skills Required

  • Demonstrated ability to strategically analyze data generation opportunities with minimal supervision
  • Ability to develop and sustain high-performing relationships with external thought leaders and internal matrix stakeholders
  • Adeptness at building credibility with external investigators and collaborative partners
  • Competent balance of business and scientific acumen
  • Strong leadership behaviors, authenticity, agility, and an enterprise mindset
  • Understanding of global healthcare systems and academic settings
  • Ability to lead in ambiguous and changing healthcare/business environments
  • Exceptional communication and interpersonal skills to influence decision-making at all levels of the organization
  • In-depth knowledge of overall project planning and project management of clinical trials
  • Proven ability to partner effectively with colleagues across multiple functions and at all levels of the enterprise
  • Expertly leverage effective communication and negotiation skills to influence decisions

Benefits & Perks

  • 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
  • Summer hours flexibility
  • Support for people with disabilities

Additional Requirements

  • Expected 20%-30% travel globally

Locations

  • Princeton NJ, United States
  • Madison Giralda NJ, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

250,000 - 350,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Demonstrated ability to strategically analyze data generation opportunities with minimal supervisionintermediate
  • Ability to develop and sustain high-performing relationships with external thought leaders and internal matrix stakeholdersintermediate
  • Adeptness at building credibility with external investigators and collaborative partnersintermediate
  • Competent balance of business and scientific acumenintermediate
  • Strong leadership behaviors, authenticity, agility, and an enterprise mindsetintermediate
  • Understanding of global healthcare systems and academic settingsintermediate
  • Ability to lead in ambiguous and changing healthcare/business environmentsintermediate
  • Exceptional communication and interpersonal skills to influence decision-making at all levels of the organizationintermediate
  • In-depth knowledge of overall project planning and project management of clinical trialsintermediate
  • Proven ability to partner effectively with colleagues across multiple functions and at all levels of the enterpriseintermediate
  • Expertly leverage effective communication and negotiation skills to influence decisionsintermediate

Required Qualifications

  • Advanced scientific degree (MD, PhD, PharmD, MS or the equivalent) required (experience)
  • At least 5 years of experience in pharmaceutical clinical development, Medical Affairs, or relevant Commercial experience (experience)

Preferred Qualifications

  • Previous customer-facing role experience highly desirable (experience)

Responsibilities

  • Facilitate collaborative exchange between BMS and thought leaders in community practice and academia
  • Provide oversight of Medical clinical trials end-to-end including start-up, governance outcomes, contract management, execution, and study support
  • Design and drive strategies to accelerate the development of BMS's clinical development pipeline
  • Leverage external research platforms, technologies, and insights
  • Contribute to the evolution of MEG therapeutic area strategy and value proposition

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility
  • general: Support for people with disabilities

Target Your Resume for "Director, MEG Lead Immunology & Neuroscience, Medical Evidence Generation" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Director, MEG Lead Immunology & Neuroscience, Medical Evidence Generation. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Director, MEG Lead Immunology & Neuroscience, Medical Evidence Generation" , Bristol-Myers Squibb

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

PharmaceuticalPharmaceuticalHealthcare

Related Jobs You May Like

No related jobs found at the moment.