Director Publications and Scientific Content, Real World and Outcomes Research

Lawrence Township, New Jersey
Commensurate with experience
May 04, 2017
Jul 05, 2017
Full Time

Director Publications and Scientific Content, Real World and Outcomes Research

Responsibilities Include:

  • Accountable for ensuring the clear, accurate and scientifically rigorous communication of BMS real world/outcomes research information for Opdivo. This role will report to the Lead, WW Real World/Outcomes Research Publications and Content
  • Engages with key internal stakeholders to facilitate early identification of anticipated data disclosures that may be relevant enabling timely preparation of other data dependent communications
  • Delivers strategically aligned scientific content including slide decks, MI letters, dossier on RW/OR data in partnership with WWHEOR leads, Access leads, Field Medical Communication Liaison RW/OR and HQ Medical leads working collaboratively across key functions and markets
  • Delivers strategically aligned publication plans and timely journal submissions/publications and congress presentations of RW/OR data in partnership with WWHEOR leads, WW Pubs/Content leads and HQ Medical Leads
  • Implements effective & consistent strategies for engaging matrix teams and external authors to advise on & shape publication plan strategy
  • Establishes and regularly communicating clear metrics aligned to meeting customer needs and demonstrating desired outcomes of activities
  • Manages 3rd-party providers to ensure the timely delivery of quality publications and scientific content
  • Reviews publication drafts for scientific quality and to ensure alignment & consistency with author direction, scientific communication platform & key communication points supported by data
  • Manages and prioritizes multiple projects, provides solutions to complex problems, and delivers complete and accurate information within deadlines
  • Partners with Operations & Execution Leads to assess, plan, and allocate resources (budget, medical writing, biostatistical services) to ensure timely delivery of high quality communications
  • Fosters collaborative relationships with publishers of outcomes research journals, medical associations & other relevant stakeholder groups
  • Monitors the external medical and scientific information landscape, identifying trends in content inquiry and aligning and adjusting to relevant trends to better meet customer needs through internal process improvements
  • Maintains awareness of applicable legal, regulatory and compliance framework and good research/publication practices applicable to health economics and outcomes research
  • Ensures compliance with internal and external standards and models good publication practices and principles among authors and internal publication stakeholder community ensuring all publications are being authored, written, and reviewed according to GPP3 and BMS processes
  • The scope of role will initially be limited to 1 tumor type or pan-tumor value activities but may be expanded to other tumor types in future as team grows. While the role currently does not have direct reports, it is expected to have direct reports in future
  • In the case of an alliance partnership, responsible for establishing work plan and building relationships necessary for success

Desired Background, Knowledge and Experience:

  • Advanced degree: Clinical/Science degree required; MS in health economics/epidemiology preferred; Scientific expertise in oncology preferred
  • A minimum of 8 years experience within the pharmaceutical or related healthcare industry
  • Experience in developing scientific publication/content strategy, planning and execution
  • Experience working in highly matrix environment across a broad range of functional areas and collaborating with the Medical Affairs, HEOR, R&D, regulatory, legal, access and commercial teams
  • Awareness of introductory health economics and outcomes research, comparative effectiveness research (CER), health technology assessment (HTA) landscape and reporting requirements
  • Ability to review, assess and synthesize CER, health outcomes and pharmacoeconomic evidence
  • Understanding of good publication practices and guidance (GPP3, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication desirable
  • Outstanding interpersonal, written and verbal communication skills with exceptional time management skills are required for this highly visible global position
  • Working knowledge of Microsoft Suite applications and familiarity with publication management tools & systems (Datavision) preferred

Bristol-Myers Squibb is a global BioPharma company firmly focused on its Mission to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. Our Oncology pipeline is one of the best in the industry and having an elite team in place is critical to our success. Bristol-Myers Squibb takes a vested interest in developing our people for not only today but for the long term and offers a range of programs to assist employees in achieving their professional and personal goals. We are consistently recognized for our diverse workforce and culture of inclusion, which are key to enhancing innovation.

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, disability or protected veteran status.