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Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Associate Director - Global Immunology & Cardiovascular Medical Communications, Rheumatology

Biology & BiotechUpdated on Nov 13
Full-timePrinceton, NJ, USA

About the Job

Requirements

  • An advanced scientific degree, PharmD, PhD, or MD is preferred.
  • Seven to ten years of pharmaceutical or healthcare industry experience focused on medical communications; experience in both local country and global settings is preferred.
  • Experience working across large or multiple teams and leading teams to high performance.
  • Ability to lead strategically, drive performance, build alignment, inform, negotiate, and collaborate.
  • Ability to work in an ambiguous environment and develop teams focused on quick deliverables.
  • Experience leading cross-functional, cross-cultural project teams and collaborating across matrix organizations, multiple markets, and global geographies.
  • Demonstrated success driving business results in a large, complex corporate environment with multiple priorities and tight timelines.
  • Ability to manage timelines and work quality using leadership, organizational, communication, facilitation, and interpersonal skills.
  • Experience establishing strategic direction for teams and achieving objectives; ability to take educated risks, rise above technical expertise, and demonstrate sound judgment and understanding of impact.
  • Experience with change leadership and leading teams through change.
  • Experience leading medical communications across all phases of drug development and commercialization.
  • Ability to analyze and interpret trial data.
  • Ability to influence, negotiate appropriate solutions, and establish strong stakeholder relationships.
  • Ability to travel.
  • Knowledge of the pharmaceutical or healthcare industry.
  • Knowledge of external compliance, transparency, and conflict-of-interest regulated work environments.
  • In-depth knowledge of Good Publication Practices and guidance (GPP, ICMJE), the Sunshine Act, the Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication.
  • Understanding of clinical trial design and execution, statistical methods, and clinical trial data reporting requirements.
  • Working knowledge of Microsoft applications and familiarity with the iEnvision publication management tool.

Responsibilities

  • Establish a clear, viable, and compelling Medical Communications strategy aligned with the overall Medical vision, strategy, and objectives.
  • Understand communication needs across markets and own the pull-through and execution of the Scientific Narrative, development and execution of the functionally integrated publication plan and content plan, and application to the Scientific Communication Platform (SCP).
  • Oversee development and execution of functionally integrated and aligned medical communications plans, adjusting them in accordance with clinical trial results and milestones and changes in the healthcare landscape.
  • Manage the Medical Communications budget and allocation of funds and resources to business priorities, interfacing with matrix partners to make trade-off decisions.
  • Lead development of medical communications, including timely journal submissions, publications, congress presentations, and delivery of internal and external scientific content.
  • Serve as a subject matter expert for internal audiences on the communication landscape, healthcare professional preferences, publication and scientific content planning, and data disclosure and dissemination; represent BMS scientific communications to external investigators, key authors, and journal editors.
  • Lead internal process improvements and transformation efforts to maintain ethical and credible publication and scientific-content practices, align standards with Good Publication Practices and industry standards, and ensure employees involved in publication activities follow those practices with integrity, quality, and transparency.
  • Apply scientific and research expertise to establish collaborations with internal and external disease-area experts and support quality data analysis, interpretation, communication planning, and data disclosure and dissemination.
  • Apply insights to medical communication to enable impactful dialogue and customer interactions.
  • Identify and drive opportunities to enhance processes, tools, operating procedures, and outsourcing strategy to ensure consistent delivery and alignment of standards.
  • Foster collaborative relationships with academic and clinical experts, publishers, medical associations, and other stakeholders; participate in external initiatives that foster trust and respect in the academic and medical publishing community.
  • Collaborate with internal Medical stakeholders, including country and regional medical directors, and teams such as Customer Engagement, Field Medical Excellence, Congress Strategy, and Training & Compliance, using external insights to inform medical communications planning.
  • Partner with third-party vendors to ensure an appropriate balance of internal and external work execution.
  • Establish metrics aligned to customer needs and desired activity outcomes, and regularly communicate the metrics to key stakeholders.

Desired Qualifications

  • Experience in both local country and global pharmaceutical or healthcare industry settings.
  • Certified Medical Publication Professional (CMPP) certification and active ISMPP membership are highly desired.

About the Company

Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Bristol Myers Squibb discovers, develops and sells prescription medicines for serious illnesses, including cancer, blood disorders, immune diseases and heart disease, for patients treated by doctors and hospitals around the world. Its best-known drug is Opdivo, an immunotherapy that helps the body's own immune system find and attack many kinds of cancer. Researchers develop drug candidates in its labs or bring them in through acquisitions and partnerships, then test them in clinical trials to win regulatory approval. The company makes and markets the approved medicines and earns its revenue from sales of patent-protected drugs. Its roots go back to a business founded in 1887, and it is based in Lawrence Township, New Jersey.

Company size
10,001+
Company stage
IPO
Headquarters
Lawrence Township, NJ
Founded
1887

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