Director, MEG Lead Oncology, Medical Evidence Generation
Bristol-Myers Squibb
Director, MEG Lead Oncology, Medical Evidence Generation
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 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, or PharmD or the equivalent) required with extensive, relevant scientific, and/or clinical experience. At least 7 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 30% travel globally
About the Role/Company
- Supporting People with Disabilities
Key Responsibilities
- Facilitate collaborative exchange between BMS and thought leaders in community practice and academia
- Represent BMS as a trusted, inclusive, and innovative industry collaborator and partner of choice
- 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
Required Qualifications
- Advanced scientific degree (MD, PhD, or PharmD or the equivalent) required
- At least 7 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
- 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
- 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
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
Additional Requirements
- Expected 30% travel globally
Locations
- Princeton NJ, United States
- Boudry, Switzerland
- Madison Giralda NJ, United States
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
250,000 - 400,000 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
- Demonstrated 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
- Competently balancing business and scientific acumen complemented by strong leadership behaviors, authenticity, agility, and an enterprise mindsetintermediate
- Understanding of global healthcare systems and academic settingsintermediate
- Demonstrated 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
- Exceptional interpersonal and communication skills appropriately flexing based on audienceintermediate
- Expertly leverages effective communication and negotiation skills to influence decisionsintermediate
Required Qualifications
- Advanced scientific degree (MD, PhD, or PharmD or the equivalent) required (experience)
- At least 7 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
- Represent BMS as a trusted, inclusive, and innovative industry collaborator and partner of choice
- 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
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
Tags & Categories
Director, MEG Lead Oncology, Medical Evidence Generation
Bristol-Myers Squibb
Director, MEG Lead Oncology, Medical Evidence Generation
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 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, or PharmD or the equivalent) required with extensive, relevant scientific, and/or clinical experience. At least 7 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 30% travel globally
About the Role/Company
- Supporting People with Disabilities
Key Responsibilities
- Facilitate collaborative exchange between BMS and thought leaders in community practice and academia
- Represent BMS as a trusted, inclusive, and innovative industry collaborator and partner of choice
- 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
Required Qualifications
- Advanced scientific degree (MD, PhD, or PharmD or the equivalent) required
- At least 7 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
- 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
- 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
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
Additional Requirements
- Expected 30% travel globally
Locations
- Princeton NJ, United States
- Boudry, Switzerland
- Madison Giralda NJ, United States
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
250,000 - 400,000 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
- Demonstrated 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
- Competently balancing business and scientific acumen complemented by strong leadership behaviors, authenticity, agility, and an enterprise mindsetintermediate
- Understanding of global healthcare systems and academic settingsintermediate
- Demonstrated 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
- Exceptional interpersonal and communication skills appropriately flexing based on audienceintermediate
- Expertly leverages effective communication and negotiation skills to influence decisionsintermediate
Required Qualifications
- Advanced scientific degree (MD, PhD, or PharmD or the equivalent) required (experience)
- At least 7 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
- Represent BMS as a trusted, inclusive, and innovative industry collaborator and partner of choice
- 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
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
Tags & Categories