Associate Director, Cell Therapy, Medical Communications Specialist

vor 2 Wochen


Boudry District, Schweiz Bristol Myers Squibb Vollzeit

About This Role

Bristol Myers Squibb is a leading biopharmaceutical company that is transforming the lives of patients with innovative medicines. We are seeking an experienced Associate Director to join our Cell Therapy team as a Medical Communications Specialist.

Key Responsibilities

  • Develop and execute medical communications strategies to ensure the disclosure of science and health economic value of BMS products and research data to inform Healthcare Providers, Patients, and Payers in accordance with local regulations.
  • Establish a clear, viable, and compelling strategy for Medical Communications, aligned with overall Medical vision, strategy, and objectives.
  • Lead the development of medical communications and ensure timely journal submissions, publications, congress presentations, and delivery of internal and external scientific content.
  • Manage Medical Communications budget and allocation of funds and resources to highest business priorities.
  • 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.
  • Lead internal process improvements to ensure BMS remains an ethical and credible leader in the practice of publications & scientific content; lead transformation efforts and ensure BMS publication & scientific content standards are aligned with Good Publication Practices and industry standards.
  • Provide oversight to the team for the development and execution of functionally integrated and aligned medical communications plans; adjust communications plans in accordance with clinical trial results/milestones and changes in the healthcare landscape.
  • Demonstrate scientific/research 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.
  • Ensure collection of insights to deliver high-quality medical communication that enables the most impactful dialogue and interactions with customers.
  • Identify and drive opportunities to enhance processes, tools, operating procedures, and outsourcing strategy to ensure consistent delivery and alignment of standards.

Requirements

  • Advanced scientific degree, PharmD, PhD, or MD preferred.
  • 7-10 years of Pharmaceutical/Healthcare industry experience with a focus on medical communications; experience in both local country & global preferred.
  • Experience of leading a large team or multiple teams; and demonstrated strength in leading teams to high performance.
  • Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate, and collaborate.
  • Proven ability to work in an ambiguous environment, and develop teams with a focus on quick deliverables.
  • Experience leading cross-functional, cross-cultural project teams, and collaborating across matrix, multiple markets, and global geographies.
  • 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.
  • Proven experience establishing strategic direction for teams, and proven ability to achieve set objectives; ability to take educated risk, rise above technical expertise; demonstrating judgement, wisdom, and understanding of impact.
  • Experience with change leadership and appreciation for complexity of 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 and negotiate appropriate solutions; ability to establish strong stakeholder relationships.
  • Ability to travel.

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).


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