Bristol Myers Squibb
Senior Manager, Multiple Myeloma MedComms
Bristol Myers Squibb, Princeton, New Jersey, us, 08543
Senior Manager, Multiple Myeloma MedComms
Join to apply for the
Senior Manager, Multiple Myeloma MedComms
role at
Bristol Myers Squibb .
Working with us creates challenging, meaningful, life‑changing opportunities. Bristol Myers Squibb’s work transforms patients’ lives and the careers of those who do it. You will grow through uncommon scale and scope alongside high‑achieving teams.
Position Summary Position reports to the Director of Medical Communications within WWMH of Global Medical Affairs. The Senior Manager plans and executes scientifically accurate, strategically aligned communications that support medical communication needs related to the specified asset(s) in WWMH.
Key Responsibilities Medical Communications Strategy
Leads across the BMS matrix to develop and timely deliver strategically aligned medical publications, scientific content, medical information, medical education, training content, and congress presentations.
Ensures endorsement of medical communications plans by relevant governance bodies prior to execution, and continuously develops and maintains plans in conjunction with scientific landscape and in alignment with Local Market Medical, Worldwide (WW) Medical and medical market‑level strategy.
Serves as the Medical Communications point of contact between WW/ and other matrix partners.
Provides medical communications management oversight.
Enhances bi‑directional communication by understanding and sharing the WW medical communications plans to Medical and raises needs to WW Medical/Medical Communications teams, ensuring country/global level of awareness & connectivity including vendor oversight.
Understands the communication needs and owns the pull‑through and execution of the Scientific Narrative, development & execution of functionally integrated publication plan, content plan, and application to the Scientific Communication Platform (SCP).
Must have strong business acumen, ability to interface with market matrix partners & manage Medical Communications budget.
Data Dissemination
Serve as a subject matter expert to BMS internal audiences related to communication landscape, HCP preferences, publication and scientific content planning, data disclosure / dissemination, and represent BMS scientific communications to external investigators, key authors and journal editors.
Promotes and reinforces principles among authors and internal publication stakeholder community, ensuring publications are authored, written, and reviewed according to publication best practices and BMS standards and policies.
Demonstrates understanding of therapeutic disease areas, expertise to support the establishment of strong working collaborations with both internal and external disease‑area experts to ensure quality data analysis, interpretation, communication planning & data disclosure / dissemination.
Ensures collection of insights to deliver high quality medical communication that enables the most impactful dialogue and interactions with customers.
Identifies and drives opportunities to enhance processes, tools, operating procedures, and outsourcing strategy to ensure consistent delivery and alignment of standards.
Stakeholder Engagement
Fostering collaborative relationships with academic & clinical experts, publishers, medical associations & other relevant key stakeholder groups; participating in external initiatives to foster trust and respect amongst academic and medical publishing community.
Partners with TA Medical Communication Leads, Market Medical and other stakeholder to assess, plan, and allocate resources (budget, medical writing, biostatistical services) to ensure timely delivery of high‑quality medical communications.
Partners externally with 3rd party vendors to ensure the appropriate balance of internal and external execution of work.
Establishes clear metrics aligned & regularly communicates metrics with key medical stakeholders.
Other Responsibilities
High performing, externally focused which emphasizes teamwork, cooperation, personal accountability, and a commitment to quality; models BMS behaviors and reinforces such behaviors at all levels in the organization.
Serve as mentor to other leads.
Ensure preparation for audit and inspection readiness.
Ensuring diversity and inclusion in decision making, organization and talent development.
Qualifications & Experience
Advance scientific degree, PharmD, PhD or MD preferred.
5+ years of Pharmaceutical/Healthcare industry experience with a focus on medical communications; experience in both local country & global preferred.
Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate and collaborate.
Experience working cross‑functional, with cross‑cultural project teams, and collaborating across matrix, markets and global geographies.
Proven ability to work in an ambiguous environment & demonstrated success driving optimal business results in a large complex corporate environment with multiple priorities and tight timelines.
Ability to manage timelines and quality of work using strong leadership, organizational, communication, facilitation and interpersonal skills.
Outstanding interpersonal, written, and verbal communication skills with exceptional time management skills.
Experience leading medical communications across all phases of drug development and commercialization.
Ability to analyze and interpret trial data.
Ability to influence and negotiate appropriate solutions; ability to establish strong stakeholder relationships.
Ability to flexibly schedule and participate in teleconferences and virtual meetings across different time zones.
Ability to travel (domestically and internationally).
Knowledge Desired
Pharmaceutical/Healthcare Industry.
External compliance, transparency and conflict‑of‑interest regulated work environments.
In‑depth knowledge of Good Publication Practices and guidance (GPP, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post‑marketing practices and scientific data communication.
Certified Medical Publication Professional (CMPP), and ISMPP active member highly desired.
Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements.
Working knowledge of Microsoft suite of applications, and familiar with publication management tool (DataVision).
Compensation Overview Madison - Giralda - NJ $135,750 - $164,491
Princeton - NJ $135,750 - $164,491
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. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
We encourage qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
We are 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, please direct inquiries to adastaffingsupport@bms.com.
We will never request payments, financial information, or social security numbers during our application or recruitment process.
We will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
We are committed to equal employment opportunity. All qualified applicants, including persons with disabilities, are encouraged to apply.
At Bristol Myers Squibb, people are empowered to apply their 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.
Candidate Rights
– BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
We will never request payments, financial information, or social security numbers during our application or recruitment process.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Use of your personal information in the context of this recruitment shall be governed by BMS’s Privacy Statement and applicable privacy laws.
Location: Princeton, NJ or remote within United States, depending on business needs.
We strongly encourage qualified individuals to apply. Do not hesitate to reach out for assistance if you need accommodations during the application process.
Thank you for your interest in Bristol Myers Squibb.
#J-18808-Ljbffr
Senior Manager, Multiple Myeloma MedComms
role at
Bristol Myers Squibb .
Working with us creates challenging, meaningful, life‑changing opportunities. Bristol Myers Squibb’s work transforms patients’ lives and the careers of those who do it. You will grow through uncommon scale and scope alongside high‑achieving teams.
Position Summary Position reports to the Director of Medical Communications within WWMH of Global Medical Affairs. The Senior Manager plans and executes scientifically accurate, strategically aligned communications that support medical communication needs related to the specified asset(s) in WWMH.
Key Responsibilities Medical Communications Strategy
Leads across the BMS matrix to develop and timely deliver strategically aligned medical publications, scientific content, medical information, medical education, training content, and congress presentations.
Ensures endorsement of medical communications plans by relevant governance bodies prior to execution, and continuously develops and maintains plans in conjunction with scientific landscape and in alignment with Local Market Medical, Worldwide (WW) Medical and medical market‑level strategy.
Serves as the Medical Communications point of contact between WW/ and other matrix partners.
Provides medical communications management oversight.
Enhances bi‑directional communication by understanding and sharing the WW medical communications plans to Medical and raises needs to WW Medical/Medical Communications teams, ensuring country/global level of awareness & connectivity including vendor oversight.
Understands the communication needs and owns the pull‑through and execution of the Scientific Narrative, development & execution of functionally integrated publication plan, content plan, and application to the Scientific Communication Platform (SCP).
Must have strong business acumen, ability to interface with market matrix partners & manage Medical Communications budget.
Data Dissemination
Serve as a subject matter expert to BMS internal audiences related to communication landscape, HCP preferences, publication and scientific content planning, data disclosure / dissemination, and represent BMS scientific communications to external investigators, key authors and journal editors.
Promotes and reinforces principles among authors and internal publication stakeholder community, ensuring publications are authored, written, and reviewed according to publication best practices and BMS standards and policies.
Demonstrates understanding of therapeutic disease areas, expertise to support the establishment of strong working collaborations with both internal and external disease‑area experts to ensure quality data analysis, interpretation, communication planning & data disclosure / dissemination.
Ensures collection of insights to deliver high quality medical communication that enables the most impactful dialogue and interactions with customers.
Identifies and drives opportunities to enhance processes, tools, operating procedures, and outsourcing strategy to ensure consistent delivery and alignment of standards.
Stakeholder Engagement
Fostering collaborative relationships with academic & clinical experts, publishers, medical associations & other relevant key stakeholder groups; participating in external initiatives to foster trust and respect amongst academic and medical publishing community.
Partners with TA Medical Communication Leads, Market Medical and other stakeholder to assess, plan, and allocate resources (budget, medical writing, biostatistical services) to ensure timely delivery of high‑quality medical communications.
Partners externally with 3rd party vendors to ensure the appropriate balance of internal and external execution of work.
Establishes clear metrics aligned & regularly communicates metrics with key medical stakeholders.
Other Responsibilities
High performing, externally focused which emphasizes teamwork, cooperation, personal accountability, and a commitment to quality; models BMS behaviors and reinforces such behaviors at all levels in the organization.
Serve as mentor to other leads.
Ensure preparation for audit and inspection readiness.
Ensuring diversity and inclusion in decision making, organization and talent development.
Qualifications & Experience
Advance scientific degree, PharmD, PhD or MD preferred.
5+ years of Pharmaceutical/Healthcare industry experience with a focus on medical communications; experience in both local country & global preferred.
Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate and collaborate.
Experience working cross‑functional, with cross‑cultural project teams, and collaborating across matrix, markets and global geographies.
Proven ability to work in an ambiguous environment & demonstrated success driving optimal business results in a large complex corporate environment with multiple priorities and tight timelines.
Ability to manage timelines and quality of work using strong leadership, organizational, communication, facilitation and interpersonal skills.
Outstanding interpersonal, written, and verbal communication skills with exceptional time management skills.
Experience leading medical communications across all phases of drug development and commercialization.
Ability to analyze and interpret trial data.
Ability to influence and negotiate appropriate solutions; ability to establish strong stakeholder relationships.
Ability to flexibly schedule and participate in teleconferences and virtual meetings across different time zones.
Ability to travel (domestically and internationally).
Knowledge Desired
Pharmaceutical/Healthcare Industry.
External compliance, transparency and conflict‑of‑interest regulated work environments.
In‑depth knowledge of Good Publication Practices and guidance (GPP, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post‑marketing practices and scientific data communication.
Certified Medical Publication Professional (CMPP), and ISMPP active member highly desired.
Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements.
Working knowledge of Microsoft suite of applications, and familiar with publication management tool (DataVision).
Compensation Overview Madison - Giralda - NJ $135,750 - $164,491
Princeton - NJ $135,750 - $164,491
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. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
We encourage qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
We are 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, please direct inquiries to adastaffingsupport@bms.com.
We will never request payments, financial information, or social security numbers during our application or recruitment process.
We will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
We are committed to equal employment opportunity. All qualified applicants, including persons with disabilities, are encouraged to apply.
At Bristol Myers Squibb, people are empowered to apply their 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.
Candidate Rights
– BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
We will never request payments, financial information, or social security numbers during our application or recruitment process.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Use of your personal information in the context of this recruitment shall be governed by BMS’s Privacy Statement and applicable privacy laws.
Location: Princeton, NJ or remote within United States, depending on business needs.
We strongly encourage qualified individuals to apply. Do not hesitate to reach out for assistance if you need accommodations during the application process.
Thank you for your interest in Bristol Myers Squibb.
#J-18808-Ljbffr