Bristol Myers Squibb Associate Director, Worldwide Hematology/Cell Therapy Scientific Publications, CAR T Lymphoma in Summit, New Jersey
At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.
The vision for WW Scientific Publications is to be strategic leaders driving scientific publications with innovative approaches to advance understanding of the science and maximize value for customers. Position reports to the Director, WW Scientific Publications, CAR T cell therapy within Medical Capabilities of Global Medical Affairs and is responsible for the strategy and execution of BMS Cell Therapy (Lymphoma) scientific publications worldwide. The Associate Director, WW Scientific Publications, Cell Therapy (Lymphoma) will ensure the disclosure of the science of BMS products and research data to inform Healthcare Providers and Patients worldwide.
A core member of the Worldwide Hematology/Cell Therapy Scientific Publications Team, the Associate Director (Cell Therapy, Lymphoma) will be accountable for:
Manages across a global matrix organization to drive quality planning and timely communication of key scientific data, clinical information, and real-world evidence (RWE) for BMS products within specified therapeutic area.
Drives strategic publication planning and provides oversight for publication strategy of assigned therapeutic area and assets.
Builds strong cross-functional collaborations and ensures alignment of the scientific communication plan with both the research and business plan for the therapeutic area.
Provides expert scientific guidance and support to cross-functional colleagues.
Demonstrates scientific and functional expertise to support the establishment of strong working collaborations with both internal and external disease area experts to ensure quality data analysis, interpretation, and communication planning.
Ensures timely publication and global communication of key data at congresses and in high-tier journals that comply with laws, regulations, and guidelines.
Leads and directs the development of publications, and reviews and approves manuscripts, abstracts, posters, and other documents to ensure appropriate evaluation and presentation of data, methodology, interpretation.
Assists Director by representing Scientific Publications at intra- and interdepartmental meetings, participating in decisions that impact the overall medical/scientific support of products within the therapeutic and asset teams.
Collaborates with internal stakeholders across the matrix and other Medical Capabilities leadership (e.g., Scientific Content, Customer Engagement, Field Medical Excellence, Compliance & Governance) to ensure efficiency and value.
Partners externally with 3rd party vendors to ensure the appropriate balance of internal and external execution of work.
Manages annual budget and works within allocated resources.
Qualifications & Experience
Advance scientific degree, PhD, MD or PharmD preferred
A minimum of 5 years of experience in the Pharmaceutical/Healthcare industry with a focus on scientific publications; experience in hematology and CAR T cell therapy preferred
Expertise across all aspects of scientific publication strategy, planning, and execution during all phases of drug development and commercialization process
Demonstrated track record of leading and executing in a highly matrixed environment working across multiple functional areas
Knowledge of Good Publication Practice, ICMJE criteria for authorship, and other relevant publication guidelines
Certified Medical Publication Professional (CMPP) and ISMPP active member highly desired
Outstanding interpersonal, written, and verbal communication skills
Ability to travel (domestically and internationally) approximately 15-20% of the time
Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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.
Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to email@example.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Company: Bristol Myers Squibb
Req Number: R1546644
Updated: 2021-09-19 01:18:12.484 UTC
Location: Summit,New Jersey
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.