The position is responsible for supporting the development and execution of harmonized global publication plans across selected mature in-line therapeutic areas at CSL Behring.
This includes author interactions, writing, and vendor management in conjunction with Good Publication Practices, internal guidance documents, and requires effective cross-functional alignment during the planning process and communication during all portions of execution of the plans.
Responsibilities:Partners with Medical TA leads and Pubs Director to develop strategic publication plans for select mature in-line products.Responsible for execution of assigned publications according to timelines of the publication plans and vendor management relating to assigned publications.Actively engage internal and external authors and other key stakeholders in the development of publication plans and strategy at the individual dataset, study, and/or compound level.With guidance of Pubs Director, ensure execution of scientific publication writing including abstracts, posters/oral presentations and manuscript in compliance with standard operating procedures/industry standards.Follow international guidelines including but not limited to International Committee of Medical Journal Editors (ICJME), Good Publication Practices (GPP), CONSORT Guidelines, American Medical Association (AMA) Manual of Style, and Council of Biology Editors.Participate in the development and maintenance of document templates, style guides, electronic document management and publication review and approval system.Ensure utilization of the PubsHub globally for publication-related activities for the responsible products.Provide oversight of completed, ongoing and future publications and manage a publication tracker for assigned products.Ensure appropriate copyright is obtained for all MA related assets. Qualifications:Degree in nursing, pharmacy or advanced degree in science/medicine (MD, PhD, Pharm D, MS) preferred with 7+ years of relevant pharmaceutical/biopharmaceutical industry or relevant experience.Experience working in matrixed teams in a global organization.Experience in biomedical research, scientific analysis and writing.Experience in vendor management.Project management experience is a plus. #J-18808-Ljbffr