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Director, GMA Oncology
3 months ago
Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. Under the Group's 2025 Vision to become a "Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
Summary
Director, Global Medical Affairs Oncology Publications works with Cross Functional Team to develop strategic publication plans, drive the execution of publication projects of assigned products, and support other GMA Oncology activities as needed.
Responsibilities
Collaborate with Global and Regional Medical Affairs, co-development company and various cross functional teams to develop publication plans of assigned GMA Oncology products
Manage timelines of publication outputFacilitate study Publication Committee discussionsLiaise with internal & external authors, academic research organizations, and study investigatorsManage vendor budget and activitiesOversee the quality and timeline of vendor workCollaborate with study medical lead and biostat to ensure availability of necessary dataCoordinate author review/approval & internal review approvalSubmit abstract/manuscripts with vendor supportFacilitate response to journal reviewer comments/requestsTrack publication tracking and announcements, in coordination with MI/ELeads the planning and execution to ensure high quality and timely delivery of scientific publicationsManages publication activities in Datavision publication management software, including internal and external review and collection of authorship agreements, financial disclosures and author approvalsEnsures documentation of compliance with authorship and publication guidelines as stipulated by the International Committee of Medical Journal Editors (ICMJE) and Good Publication Practice for Communicating Company-Sponsored Medical Research (GPP)Works with and oversee publication vendors to ensure deliverables are of high quality, delivered in a timely manner, and in budget.Liaises with internal and external stakeholder, co-development company, including authors, researchers, investigators, GMA medical leads, R&D clinical leads, bio stats and Publications Committee members on publication activitiesLeads study publication committee discussions, including monthly, quarterly and yearly publication update meetings as neededSupport global medical communication plan development by collaborating with GMA team including co-development companySupport other global data dissemination activities as needed• Align with the Head of Publications Oncology and respective team members to ensure robust publication plans for the Therapeutic Area and respective products. Mentor Associate Director Publication leads on publication planning and execution related matters.Lead and facilitate Publication Review Committee(s) discussion. Coordinate author review/approval and internal review approval of manuscripts, abstracts, poster presentations, and oral presentations related to the brand(s).Manage vendor budget and activities and oversee the quality and timeline of vendor work
Manage Publication tracking and announcement, in coordination with Medical Director and Medical Information /Education function
Contribute to development of medical communication plan budget (i.e. Publications, Medical Slides, and other related projects). Collaborate with Medical Director responsible for Communication Strategy and Medical Program Management on tracking and management of budget.Support Head of Publications- Oncology by assisting with department initiatives:Assist in enhancing processes, procedures, and workflow strategies across the publication teamReview of publication tools and databases to determine the best technologies to enhance publication workflowPartner internally to capture timely metrics and Key Performance Indicators based reportingAssist in department wide publications initiatives as needed.Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.Education Qualifications (from an accredited college or university)Bachelor's Degree or Advanced Degree in Health Sciences may be considered based on years of experience/qualifications requiredMaster's Degree Advanced Degree in Health Sciences may be considered based on years of experience/qualifications preferredPharmD or PhD in Health Sciences preferredExperience Qualifications7 or More Years of pharmaceutical industry, clinical, and/or academic experience for PharmD, or PhD required7 or More Years of pharmaceutical industry experience required or10 or More Years with publication/communication agency for Bachelors or MS degree in health sciences requiredProven tack record of working successfully with cross functional teams to achieve goals preferredExperience with publication planning requiredExperience with clinical trials and international work experience preferredTravelAbility to travel up to 20%Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
