Emeryville, CA, 94662, USA
3 days ago
Director, Solid Tumor Oncology Global Scientific Publications and Communications
**General** **Description:** The Solid Tumor Oncology Global Scientific Publications and Communications provides publications expertise and insight into the development and optimization of integrated strategic global publication plans in Solid Tumor Oncology. In this role the Director, will be responsible to develop strategic publication plans, manage and deliver scientifically rigorous and compliant publication tactics across the product lifecycles. This role has responsibility for Oncology TA-specific publications across the BeOne solid tumor Oncology portfolio. The Director will work with cross functional matrix partners and is responsible for the development of scientific communication plans and the management and execution of high quality publication tactics that align with the business needs within Medical Affairs and Clinical Development. This role reports into the Senior Director of Global Scientific Communications and Publications in Solid Tumor Oncology within Global Medical Affairs. **Essential Functions of the job:** + Manage, lead, develop, comprehensive, long term, strategic integrated Oncology publication plans which are aligned to medical objectives. + Understand the communication needs globally and across markets and own the pull through and execution of the scientific narrative, development and execution of functionally integrated scientific communication plan for publications and application to the scientific communication platform (SCP). + Works collaboratively with cross functional matrix partners and leads publication planning and strategy discussions. + Lead development of publications and ensure timely submissions to congresses and journals. + Ensures publications encompass key scientific statements that are supported by appropriate data, maximizing the impact and credibility of scientific communications. + Ensure the integrated publication strategy/plan is consistently applied across all studies and clear and supportable scientific data are communicated to internal partners (product teams, governance bodies) and external customers (regulatory authorities, payers, physicians and patients). + Serve as the TA-specific subject matter expert for BeOne internal audiences related to communication landscape, HCP preferences, publication planning, data disclosure dissemination, and represent BeOne scientific communications to external investigators, authors, alliance partners, and journal editors. + Have strong business acumen, ability to interface with matrix partners to make trade off decisions by managing asset/TA-specific budget and allocation of funds and resources. + Lead the development of medical and scientific lexicons as needed in close collaboration with cross-functional colleagues. + Provide publications expertise and insight to develop effective operating models and build effective relationships with Alliance partners as required by the business needs. + When needed, provide support to PLs working in alliances with joint venture partners and key alliance partners to ensure the right scientific and technical skills and capabilities are leveraged to drive productive relationships in support of the overall alliance strategy. **Education Required:** + Advanced degree is required (i.e. MS, Pharm.D., or PhD). **Qualifications:** + ​PhD, Pharm.D. or MS or advanced post-graduate scientific degree with relevant proven experience in pharmaceutical/medical communication/healthcare industry, development, research is required. + 8+ years within the pharmaceutical industry, a consulting organization, and/or a medical communications company; 5+ years in scientific communications/publications. + Managerial experience strongly preferred. + Demonstrated experience as a medical publication professional and in-depth knowledge of the principles of developing effective publication strategies and plans. + Demonstrated performance and resource management skills in a global organization. + Broad knowledge of the drug development process, with a focus on integrated strategic publication planning (preferred). + Broad knowledge of relevant disease areas. + Publications experience (global and regional) with demonstrated ability to work in a cross-cultural business environment. + Proven ability to set and manage multiple priorities, resources, performance targets and project initiatives in a global section and project environment. + Proven flexibility and adaptability to changing regulatory and publication environment by developing solutions that impact beyond the function. + Manages change with a positive approach to the challenges of change for self, team and the business. + Excellent written and verbal communication skills, negotiation, collaboration and interpersonal skills. + High ethical standards. **Supervisory** **Responsibilities:** + No **Computer** **Skills:** + EfficientinMicrosoftWord,Excel,PPT,andOutlook **Travel:** + 10-15%%;positionmayrequireoccasionaltravelformajormedicalconferences. All 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.
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