Senior Director, Global Medical Immunology & Cardiovascular, Milvexian Medical Strategy (MD/DO required)
Bristol-Myers Squibb
Senior Director, Global Medical Immunology & Cardiovascular, Milvexian Medical Strategy (MD/DO required)
Job Description
Support the execution of Global medical plan that is both product and disease specific, translating commercialization and medical strategies into effective milvexian medical launch plans and life cycle management plans. Works with cross-functional matrix and alliance partners on a variety of projects, provides independent thought and initiative in the further development of specific projects and ensuing presentations and status updates Identify Medical data generation strategies, collaborate with Medical Evidence Generation (MEG) to review and oversee execution of the Investigator Sponsored Research (ISR) programs Provide strategic input in Phase IIIb/IV trials and real-world evidence programs across Global Medical Affairs Review and develop study concepts, protocols and reports aligned with integrated evidence generation plans Attends major conferences and helps coordinate medical affairs activities at conferences Responsible for the development and execution of projects that will provide more extensive background, and additional data/answers to questions in response to issues relative to commercial, scientific, or data needs Serves as medical strategy point on select scientific issues/topics using expertise to develop scientific messages, inform strategy, create/update slide decks, and review scientific content and publication Collaborates with the Executive Director, Medical Product Lead and medical matrix in the development of Customer Impact Plan and ensures alignment of team activities Regular communication with external thought leaders and internal field team to identify key insights and to provide medical education, support, and direction as appropriate Partner closely with colleagues in Discovery, Clinical Research, Regulatory, and Health Outcomes to ensure the science of the pipeline products and marketed medicines are understood and communicated properly internally and externally. 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. MD/DO (Clinical Cardiology/Thrombosis Medical affairs experience preferred) Candidate should have the ability to speak English Must be familiar with all phases of drug development Healthcare landscape knowledge & insight Proven impact and influence with high impact national thought leaders Excellent analytical skills demonstrated ability to identify and understand complex issues and problems and identify and query key findings from study data and publications Organized, attention to detail and ability to meet timelines in a fast-paced environment Experience in developing effective abstracts, manuscripts, posters and slides, and presenting at scientific meetings Ability to work on multiple projects simultaneously and effectively prioritize workload Must be able to work with a level of autonomy and independence Business acumen Partnering and collaboration Influencing and persuasion- negotiation skills Verbal & written communication skills Change leadership Ability to lead and manage a complex (e.g., cross-functional, matrix designed) project team Experience with people management Travel Required: Expected 30-40% travel within the continental US and ex-US markets
About the Role/Company
- The company focuses on global medical strategy, particularly in Immunology & Cardiovascular areas, with emphasis on milvexian medical strategy
Key Responsibilities
- Support the execution of Global medical plan that is both product and disease specific
- Translate commercialization and medical strategies into effective milvexian medical launch plans and life cycle management plans
- Work with cross-functional matrix and alliance partners on a variety of projects
- Provide independent thought and initiative in the further development of specific projects and ensuing presentations and status updates
- Identify Medical data generation strategies
- Collaborate with Medical Evidence Generation (MEG) to review and oversee execution of the Investigator Sponsored Research (ISR) programs
- Provide strategic input in Phase IIIb/IV trials and real-world evidence programs across Global Medical Affairs
- Review and develop study concepts, protocols, and reports aligned with integrated evidence generation plans
- Attend major conferences and help coordinate medical affairs activities at conferences
- Develop and execute projects that provide more extensive background and additional data/answers to questions
- Serve as medical strategy point on select scientific issues/topics
- Develop scientific messages, inform strategy, create/update slide decks, and review scientific content and publication
- Collaborate with the Executive Director, Medical Product Lead and medical matrix in the development of Customer Impact Plan
- Ensure alignment of team activities
- Communicate regularly with external thought leaders and internal field team to identify key insights and provide medical education, support, and direction
- Partner closely with colleagues in Discovery, Clinical Research, Regulatory, and Health Outcomes to ensure the science of the pipeline products and marketed medicines are understood and communicated properly
Required Qualifications
- MD/DO degree required
- Familiarity with all phases of drug development
- Proven impact and influence with high impact national thought leaders
- Experience in developing effective abstracts, manuscripts, posters, and slides
- Ability to work on multiple projects simultaneously and effectively prioritize workload
- Ability to work with a level of autonomy and independence
- Experience with people management
Preferred Qualifications
- Clinical Cardiology/Thrombosis Medical affairs experience
Skills Required
- Ability to speak English
- Excellent analytical skills
- Demonstrated ability to identify and understand complex issues and problems
- Ability to identify and query key findings from study data and publications
- Organized with attention to detail
- Ability to meet timelines in a fast-paced environment
- Business acumen
- Partnering and collaboration
- Influencing and persuasion- negotiation skills
- Verbal & written communication skills
- Change leadership
- Ability to lead and manage a complex (e.g., cross-functional, matrix designed) project team
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
- Travel Required: Expected 30-40% travel within the continental US and ex-US markets
Locations
- Princeton NJ, United States
Salary
Estimated Salary Rangemedium confidence
350,000 - 550,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Ability to speak Englishintermediate
- Excellent analytical skillsintermediate
- Demonstrated ability to identify and understand complex issues and problemsintermediate
- Ability to identify and query key findings from study data and publicationsintermediate
- Organized with attention to detailintermediate
- Ability to meet timelines in a fast-paced environmentintermediate
- Business acumenintermediate
- Partnering and collaborationintermediate
- Influencing and persuasion- negotiation skillsintermediate
- Verbal & written communication skillsintermediate
- Change leadershipintermediate
- Ability to lead and manage a complex (e.g., cross-functional, matrix designed) project teamintermediate
Required Qualifications
- MD/DO degree required (experience)
- Familiarity with all phases of drug development (experience)
- Proven impact and influence with high impact national thought leaders (experience)
- Experience in developing effective abstracts, manuscripts, posters, and slides (experience)
- Ability to work on multiple projects simultaneously and effectively prioritize workload (experience)
- Ability to work with a level of autonomy and independence (experience)
- Experience with people management (experience)
Preferred Qualifications
- Clinical Cardiology/Thrombosis Medical affairs experience (experience)
Responsibilities
- Support the execution of Global medical plan that is both product and disease specific
- Translate commercialization and medical strategies into effective milvexian medical launch plans and life cycle management plans
- Work with cross-functional matrix and alliance partners on a variety of projects
- Provide independent thought and initiative in the further development of specific projects and ensuing presentations and status updates
- Identify Medical data generation strategies
- Collaborate with Medical Evidence Generation (MEG) to review and oversee execution of the Investigator Sponsored Research (ISR) programs
- Provide strategic input in Phase IIIb/IV trials and real-world evidence programs across Global Medical Affairs
- Review and develop study concepts, protocols, and reports aligned with integrated evidence generation plans
- Attend major conferences and help coordinate medical affairs activities at conferences
- Develop and execute projects that provide more extensive background and additional data/answers to questions
- Serve as medical strategy point on select scientific issues/topics
- Develop scientific messages, inform strategy, create/update slide decks, and review scientific content and publication
- Collaborate with the Executive Director, Medical Product Lead and medical matrix in the development of Customer Impact Plan
- Ensure alignment of team activities
- Communicate regularly with external thought leaders and internal field team to identify key insights and provide medical education, support, and direction
- Partner closely with colleagues in Discovery, Clinical Research, Regulatory, and Health Outcomes to ensure the science of the pipeline products and marketed medicines are understood and communicated properly
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
Travel Requirements
0%
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Senior Director, Global Medical Immunology & Cardiovascular, Milvexian Medical Strategy (MD/DO required)
Bristol-Myers Squibb
Senior Director, Global Medical Immunology & Cardiovascular, Milvexian Medical Strategy (MD/DO required)
Job Description
Support the execution of Global medical plan that is both product and disease specific, translating commercialization and medical strategies into effective milvexian medical launch plans and life cycle management plans. Works with cross-functional matrix and alliance partners on a variety of projects, provides independent thought and initiative in the further development of specific projects and ensuing presentations and status updates Identify Medical data generation strategies, collaborate with Medical Evidence Generation (MEG) to review and oversee execution of the Investigator Sponsored Research (ISR) programs Provide strategic input in Phase IIIb/IV trials and real-world evidence programs across Global Medical Affairs Review and develop study concepts, protocols and reports aligned with integrated evidence generation plans Attends major conferences and helps coordinate medical affairs activities at conferences Responsible for the development and execution of projects that will provide more extensive background, and additional data/answers to questions in response to issues relative to commercial, scientific, or data needs Serves as medical strategy point on select scientific issues/topics using expertise to develop scientific messages, inform strategy, create/update slide decks, and review scientific content and publication Collaborates with the Executive Director, Medical Product Lead and medical matrix in the development of Customer Impact Plan and ensures alignment of team activities Regular communication with external thought leaders and internal field team to identify key insights and to provide medical education, support, and direction as appropriate Partner closely with colleagues in Discovery, Clinical Research, Regulatory, and Health Outcomes to ensure the science of the pipeline products and marketed medicines are understood and communicated properly internally and externally. 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. MD/DO (Clinical Cardiology/Thrombosis Medical affairs experience preferred) Candidate should have the ability to speak English Must be familiar with all phases of drug development Healthcare landscape knowledge & insight Proven impact and influence with high impact national thought leaders Excellent analytical skills demonstrated ability to identify and understand complex issues and problems and identify and query key findings from study data and publications Organized, attention to detail and ability to meet timelines in a fast-paced environment Experience in developing effective abstracts, manuscripts, posters and slides, and presenting at scientific meetings Ability to work on multiple projects simultaneously and effectively prioritize workload Must be able to work with a level of autonomy and independence Business acumen Partnering and collaboration Influencing and persuasion- negotiation skills Verbal & written communication skills Change leadership Ability to lead and manage a complex (e.g., cross-functional, matrix designed) project team Experience with people management Travel Required: Expected 30-40% travel within the continental US and ex-US markets
About the Role/Company
- The company focuses on global medical strategy, particularly in Immunology & Cardiovascular areas, with emphasis on milvexian medical strategy
Key Responsibilities
- Support the execution of Global medical plan that is both product and disease specific
- Translate commercialization and medical strategies into effective milvexian medical launch plans and life cycle management plans
- Work with cross-functional matrix and alliance partners on a variety of projects
- Provide independent thought and initiative in the further development of specific projects and ensuing presentations and status updates
- Identify Medical data generation strategies
- Collaborate with Medical Evidence Generation (MEG) to review and oversee execution of the Investigator Sponsored Research (ISR) programs
- Provide strategic input in Phase IIIb/IV trials and real-world evidence programs across Global Medical Affairs
- Review and develop study concepts, protocols, and reports aligned with integrated evidence generation plans
- Attend major conferences and help coordinate medical affairs activities at conferences
- Develop and execute projects that provide more extensive background and additional data/answers to questions
- Serve as medical strategy point on select scientific issues/topics
- Develop scientific messages, inform strategy, create/update slide decks, and review scientific content and publication
- Collaborate with the Executive Director, Medical Product Lead and medical matrix in the development of Customer Impact Plan
- Ensure alignment of team activities
- Communicate regularly with external thought leaders and internal field team to identify key insights and provide medical education, support, and direction
- Partner closely with colleagues in Discovery, Clinical Research, Regulatory, and Health Outcomes to ensure the science of the pipeline products and marketed medicines are understood and communicated properly
Required Qualifications
- MD/DO degree required
- Familiarity with all phases of drug development
- Proven impact and influence with high impact national thought leaders
- Experience in developing effective abstracts, manuscripts, posters, and slides
- Ability to work on multiple projects simultaneously and effectively prioritize workload
- Ability to work with a level of autonomy and independence
- Experience with people management
Preferred Qualifications
- Clinical Cardiology/Thrombosis Medical affairs experience
Skills Required
- Ability to speak English
- Excellent analytical skills
- Demonstrated ability to identify and understand complex issues and problems
- Ability to identify and query key findings from study data and publications
- Organized with attention to detail
- Ability to meet timelines in a fast-paced environment
- Business acumen
- Partnering and collaboration
- Influencing and persuasion- negotiation skills
- Verbal & written communication skills
- Change leadership
- Ability to lead and manage a complex (e.g., cross-functional, matrix designed) project team
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
- Travel Required: Expected 30-40% travel within the continental US and ex-US markets
Locations
- Princeton NJ, United States
Salary
Estimated Salary Rangemedium confidence
350,000 - 550,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Ability to speak Englishintermediate
- Excellent analytical skillsintermediate
- Demonstrated ability to identify and understand complex issues and problemsintermediate
- Ability to identify and query key findings from study data and publicationsintermediate
- Organized with attention to detailintermediate
- Ability to meet timelines in a fast-paced environmentintermediate
- Business acumenintermediate
- Partnering and collaborationintermediate
- Influencing and persuasion- negotiation skillsintermediate
- Verbal & written communication skillsintermediate
- Change leadershipintermediate
- Ability to lead and manage a complex (e.g., cross-functional, matrix designed) project teamintermediate
Required Qualifications
- MD/DO degree required (experience)
- Familiarity with all phases of drug development (experience)
- Proven impact and influence with high impact national thought leaders (experience)
- Experience in developing effective abstracts, manuscripts, posters, and slides (experience)
- Ability to work on multiple projects simultaneously and effectively prioritize workload (experience)
- Ability to work with a level of autonomy and independence (experience)
- Experience with people management (experience)
Preferred Qualifications
- Clinical Cardiology/Thrombosis Medical affairs experience (experience)
Responsibilities
- Support the execution of Global medical plan that is both product and disease specific
- Translate commercialization and medical strategies into effective milvexian medical launch plans and life cycle management plans
- Work with cross-functional matrix and alliance partners on a variety of projects
- Provide independent thought and initiative in the further development of specific projects and ensuing presentations and status updates
- Identify Medical data generation strategies
- Collaborate with Medical Evidence Generation (MEG) to review and oversee execution of the Investigator Sponsored Research (ISR) programs
- Provide strategic input in Phase IIIb/IV trials and real-world evidence programs across Global Medical Affairs
- Review and develop study concepts, protocols, and reports aligned with integrated evidence generation plans
- Attend major conferences and help coordinate medical affairs activities at conferences
- Develop and execute projects that provide more extensive background and additional data/answers to questions
- Serve as medical strategy point on select scientific issues/topics
- Develop scientific messages, inform strategy, create/update slide decks, and review scientific content and publication
- Collaborate with the Executive Director, Medical Product Lead and medical matrix in the development of Customer Impact Plan
- Ensure alignment of team activities
- Communicate regularly with external thought leaders and internal field team to identify key insights and provide medical education, support, and direction
- Partner closely with colleagues in Discovery, Clinical Research, Regulatory, and Health Outcomes to ensure the science of the pipeline products and marketed medicines are understood and communicated properly
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
Travel Requirements
0%
Tags & Categories
Answer 10 quick questions to check your fit for Senior Director, Global Medical Immunology & Cardiovascular, Milvexian Medical Strategy (MD/DO required) @ Bristol-Myers Squibb.
10 Questions
~2 Minutes
Instant Score
Related Books and Jobs