Bristol-Myers Squibb Company

WW HEOR Publications and Scientific Content Manager, Innovative Medicines (Eliquis)

Location
Princeton, NJ, US
Posted
Dec 22, 2018
Ref
R1512748
Required Education
Doctorate/PHD/MD
Position Type
Full time
Summary

The primary responsibility for the WW HEOR Publications and Scientific Content Manager, Innovative Medicines (Eliquis) is supporting the WW HEOR Publications and Scientific Content Lead, Innovative Medicines in the development and delivery of a comprehensive, globally aligned strategic publications and scientific communications plan that reflects priorities for key markets.

Responsibilities

Supports a high performing, cross-functional global communications matrix team engaged in the planning, integration, and execution of medical publication and scientific content activities globally

Works to build and demonstrate understanding of the disease area, medical strategies and objectives necessary to provide strategic input to a broad range of stakeholders on matters related to publication and scientific content planning & data dissemination/disclosure under the direct mentorship of the Global Publications and Scientific Content Leads

Employs innovative strategies and solutions to ensure timely communication of scientific data

Understands and complies with established good publication practices (GPP3 and BMS processes) to support development and maintenance of the HEOR publication plan as well as abstracts, posters, and manuscripts

Manages development of content deliverables, such as reactive materials for field medical and field HEOR use, including core slide decks, training materials, FAQs, and backgrounders to address specific unsolicited health care provider and payer requests for health economic or outcomes research (HEOR) information

Plays an active role in soliciting and understanding regional market-level insights, publications and scientific content needs and ensuring that regional markets are familiar with global publications and scientific content strategies and plans

Conducts literature searches in databases such as EMBASE and Pubmed/Medline

Analyzes and interprets scientific data to update or develop comprehensive, balanced, credible, and accurate documents

Ensures deliverables comply with applicable laws, regulations, policies and procedures

Manages and prioritizes multiple projects, provides solutions to complex problems, and delivers complete and accurate information within deadline

Maintains awareness of current industry practices that pertain to use of reactive information

Liaise with HEOR agency partner to provide direction on planned and active projects and review developed materials

Requirements

Advanced degree: PharmD, PhD, or equivalent in a science subject or biomedical degree preferred

Cardiovascular experience strongly preferred

3+ years in medical writing and relevant industry work experience; expert in medical communications

Proven ability to analyze and interpret clinical, real-world, health economics and outcomes data, and other complex information

Proven ability to develop high-quality scientific content and medical information that is communicated clearly and delivered concisely

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

Attention to detail, excellent editorial skills and familiarity with the AMA style guide

Excellent organizational skills

Strong project management and leadership skills

Highly proficient in the use of Microsoft Word and PowerPoint