Director, Oncology Solid Tumor WW Scientific Content & US Ma

Company: Adecco Group
Location: Princeton
Posted on: April 8, 2021

Job Description:

Director, Oncology Solid Tumor WW Scientific Content & US Market Capabilities

• Medical Affairs
• R1538014
• Full Time
• 2021-03-31T00:00:00+0000 mail_outlineGet future jobs matching this search or Job Description At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.--In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Key Responsibilities The primary responsibility for the WW Scientific Content and US Market Capabilities Lead, is ensuring the development and execution of a comprehensive, globally aligned strategic WW/US scientific content plans to support the effective communication of data and launch for safe and effective use of BMS medicines. Accountable for a team executing on the below responsibilities, across all solid tumors in the BMS oncology portfolio across all tumors within: GI/GU/MEL/Thoracic/Women Cancers: Develop and update US local market medical content per clinical development program, publications, data presentations, congress activity, MI inquiry trends, global communication platform, product safety reports and treatment landscape. Collaborate with cross-functional stakeholders (WW Pub leads, Country Medical Directors (CMD), Field Medical Scientists, etc. to identify pertinent data and solicit functional expertise when needed to ensure medical content is developed with a high degree of medical integrity, accuracy and clinical relevance. Lead through close partnership & in collaboration with WW & US Medical, WW Pubs, HEOR, Medical Contact Center leads, in the development of medical content. Work with cross-functional teams on a worldwide level to ensure a consistent scientific narrative and communication of medical information. Support the global standardization of Medical content to streamline creation, distribution and curation of content while eliminating redundancies in resource utilization and deliverables. Analyze and interpret scientific data to update or develop comprehensive, balanced, credible and -- accurate documents that comply with applicable laws, regulations, guidance and BMS policies and procedures. Determine extent of global content available for use in the market including self-service, and ensures local customization or de novo content generation needs are met with quality and speed. Collaborate closely with the Medical Capabilities Customer Engagement & Contact Center, to inform new content deliverables and consult on training for new data. Develop Medical Contact Center training on disease state, product overview and relevant market events to ensure Contact Center's readiness to address customer inquiries. Work effectively as a member of the US and WW Medical Matrix Teams and with other core functions by contributing to development of the Medical Plans, communicating insights and trends from WW/US Medical, WW Pubs and Field Medical and contributing to the identification and delivery of content to address WW/US Market unmet medical needs. Translate medical strategies and objectives into actionable integrated content plans for WW/US. Ensure effective rollout and communication occurs, feedback loops are implemented, and continuous improvement opportunities are identified for content development. Develop, maintain and enhance the Oncology Solid Tumor team to provide high quality medical communication support. Develop comprehensive, balanced, credible and accurate documents that are used to appropriately communicate with customers involved in evidence-based healthcare decisions including but not limited to payer organizations, access influencers, pharmacy benefit managers, specialty pharmacies, compendia publishers, guideline bodies and technology assessment entities. Comply with applicable laws, regulations, guidance's and BMS policies and procedures, Evaluate and interpret medical literature, abstract and writing medical information in various formats (formulary dossiers, medical information letters, slide presentations, compendia submissions etc.) Develop and manage the production of AMCP dossiers, content letters, and slide decks utilizing HEOR data. Matrix management across medical matrix teams/value teams and senior stakeholders Manage and prioritize multiple projects, provide solutions to complex problems, and deliver complete and accurate content and information within deadlines. Manage day to day finances, contracting and vendor agency partnership to drive planning and execution of US/WW content deliverables. Supervisory Responsibilities Attract, hire, develop, and retain a talented, diverse cohesive team. Support growth and development experiences that prepare individuals for broader responsibilities. Actively manage the professional development of direct reports by ensuring that all team members understand their individual performance targets and by helping direct reports address performance gaps. Job Requirements PharmD, MD, PhD with minimum of 5 years of experience in clinical practice or pharmaceutical industry. Expert clinical, pharmacological and pharmaceutical knowledge and thorough understanding of medical terminology, and the function, activities and processes of Medical Information. Knowledge and experience in disease areas and treatment options with scientific expertise in Oncology, preferred. Expertise of all phases of drug development and commercialization process (investigational, registration, pre & post-launch and marketed), desirable Must have experience working in highly matrix environment across a broad range of functional areas and effectively collaborating with the Medical Affairs, Health Outcomes, R&D, regulatory, legal and commercial teams. Understands the needs of health care professionals and demonstrates an understanding of pharmaceutical industry regulations. Demonstrated ability to manage various projects, solve problems, deliver on commitments, and work with multidisciplinary teams. Proficiency in basic computer programs. Excellent scientific/medical written and verbal communication skills in English required. Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. 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 with the resources to pursue their goals, both at work and in their personal lives.--
  Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Keywords: Adecco Group, Trenton , Director, Oncology Solid Tumor WW Scientific Content & US Ma, Executive , Princeton, New Jersey