Director Melanoma/GU Publications & Scientific Content

Bristol-Myers Squibb Lawrence Township, NJ

About the Job

Description:

About Bristol-Myers Squibb\:

Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

 

One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease. Empowered to apply our individual talents and ideas so that we can learn and grow together. And driven to make a difference, from innovative research to hands-on community support.  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 the resources to pursue their goals, both at work and in their personal lives.

 

Structure, Scope & Accountability\:

  • Reports to WW Head Medical Publications & Scientific Content
  • Critical role accountable for ensuring the clear, accurate and scientifically rigorous communication of BMS information that informs medical practice for drug development & commercialization
  • Responsible for publications of all BMS data generation  
  • Direct impact on the success of BMS publications (ie. timely journal submissions / publications, Congress presentations, Field Medical scientific content)
  • Accountable for aligned creation of scientific and medical information across the BMS enterprise
  • Responsible for vision, strategy and execution of medical and scientific information exchange plans/platforms; including medical publications and content
  • Sets the goals and objectives for team, working closely with full development and medical leaders
  • Leads an organization of approximately 12 full-time and contract experts, with a budget of approximately $XXM
  • Partners internally to ensure team has necessary resources
  • Makes key decisions during the publication and scientific content development process
  • In the case of partnerships/alliances, manages the relationship and takes accountability for the combined success
  • Partners internally to identify, set timing and execute data dependencies and related disclosures of information in multiple communication channels including publications & scientific content
  • Partners externally with 3rd party vendors to ensure the appropriate balance of internal and external execution of work
  • Serves as a member of the WW Medical Publications & Scientific Content leadership team
  • Evaluates, collaborates and leads the partnership with many agencies to achieve objectives
  • Works extensively with Senior Leaders across the globe (R&D, Commercial, Medical) to develop publication and content plans that support the overall strategic communications asset strategy in a very competitive environment
  • Facilitates the alignment of medical publications and scientific content plans/platforms with internal matrix stakeholders, external key opinion leaders and approval by internal governing bodies
  • Represents BMS scientific communications to external investigators, key authors and journal editors
  • Presents and maintains alignment with matrix stakeholders on accomplishments, trends and book of work
  • Identifies and drives opportunities to standardize medical publications & scientific content
  • Identifies and drives opportunities to increase value and better leverage medical publications & scientific content
  • Manages a budget

Leads team for a Melanoma/GU accountable for the following\:

  • Delivering medical publications plans, publications, congress presentations, creating medical and scientific content. Scientific content is used for BMS medical professionals, call centers and field medical teams (in scientific exchange directly)
  • Reviewing draft publications and scientific content
  • Adjusting publications and medical content plans in accordance with clinical trial results/milestones and changes in the market healthcare landscape
  • Monitoring the external medical and scientific information landscape and for leading internal process improvements to stay the leader in the field, and enable BMS to be viewed as the top partner of choice by healthcare professionals
  • Fostering collaborative relationships with academic & clinical experts, authors, publishers, medical associations & other relevant stakeholder groups; including participating in external initiatives to foster trust and respect amongst academic and medical publishing community
  • Establishing and regularly communicating clear metrics aligned to meeting customer needs and demonstrating desired outcomes of activities
  • Identifying trends in content inquiry and aligning and adjusting to relevant trends to better meet customer needs
  • Ensuring compliance with internal and external standards
  • Identifying relevant data for content requests
  • Soliciting expertise when necessary to address a content request

Collaboration\:

  • Represents the Publications & Scientific Content through collaborations with senior leaders across the enterprise on cross-functional initiatives aimed at improving the overall efficiency, effectiveness, simplification, focus and integration of the business
  • Partners with Field Medical Capabilities, Standards & Technology to align and communicate standards, playbooks, guidelines, tools and templates for a specific tumor type/therapeutic area/phase to ensure a consistent and efficient approach to the creation, management and dissemination of medical and scientific information
  • Demonstrates true medical & scientific information functional subject matter expertise & credibility (e.g, CMPP certification, ISMPP active member) to serve as an educator to internal & external audiences
  • Demonstrates scientific subject matter expertise in a specific tumor type/therapeutic area/phase

Management\:

  • Identifies, hires, develops, coaches high potential employees to ensure a rich pipeline of engaged, empowered and enriched talent
  • Creates a high performing, externally focused team which emphasizes teamwork, cooperation, personal accountability and a commitment to quality
  • Models BMS behaviors and reinforces such behaviors at all levels in the organization
  • Provides oversight and approval of partnerships with vendors and contract support to support and optimal and flexible workforce

Qualification:

Experience Desired

  • Advance scientific degree, PharmD, PhD or MD preferred
  • Certification as a Medical Publication Professional (CMPP) highly desirable
  • 7 - 10 years of Pharmaceutical/Healthcare industry experience with a focus on scientific and/or medical information
  • 5 years of leading a medical team
  • Experience leading publications and scientific content development across all phases of the drug development and commercialization process
  • Proven ability to work in an ambiguous environment, and develop a function with a focus on quick deliverables.
  • Experience collaborating across a matrix, multiple markets and global geographies
  • Experience participating in, facilitating and leading cross-functional, cross-cultural project teams
  • Demonstrated success driving optimal business results in a large complex corporate environment with multiple priorities and tight timelines
  • Demonstrated ability to manage timelines and quality of work using strong organizational, communication, facilitation and interpersonal skills in a cross-functional team
  • Ability to think strategically in a changing environment
  • Entrepreneurial skill and ability to take educated risk
  • Ability to rise above technical expertise; demonstrating judgement, wisdom and understanding of impact
  • Experience leading functions, individuals and peers through change
  • Medical writing experience
  • Ability to analyze and interpret clinical data
  • English fluency

Knowledge Desired

  • Pharmaceutical/Healthcare Industry
  • External Compliance/Transparency/Conflict-of-Interest regulated work environments
  • Good Scientific & Medical Information practice and guidance; especially publications and content standards of practice
  • Sunshine Act
  • Pharma Code of Conduct, global guidance and regulations related to post-marketing practices and scientific data communication
  • Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements