Scientific Publications Lead

il y a 3 semaines


Bruxelles, Région de Bruxelles, Belgique Oxford Global Resources Temps plein

Do you have experience with scientific publications and want to extend your experience in a Scientific Publications Lead role in a dynamic, growing Biotech company? Don't hesitate and apply now

Job Description

The Scientific Publications Lead is responsible for the strategic planning, development, and delivery of scientific, technical, and medical publications. Organizing and leading cross-functional publication teams to ensure high quality publications in full compliance with good publication practices and scientific publication quality standards, strengthening the company's external reputation. Actively promoting and driving good publication practices.

Responsibilities

Define the publications strategy and publications development plans supporting the drug development & research products. Ensure cross-functional publication teams are established for key projects in the portfolio, including all required capabilities.Lead the timely delivery of planned publications to target audiences, forging good links with experts, investigators, journal editors, research partners or partner companies (if applicable), and internal staff.Ensure scientific publications excellence, in compliance with all applicable external codes and ethical standards in publishing.Define and request necessary budget and resources related to scientific publications activities.Identify, select, and manage 3rd-party providers and independent contractors to ensure the timely delivery of quality scientific publications.Identify and address hiring, training and development needs for the scientific publications leads with functional and TA expertise.Establish and maintain operational excellence of the publication leads activities in terms of publication budget & vendor management, as well as publications management systems, etc.Develop, promote, and support good publication practices and principles (POL, SOP, WI) among authors and the internal stakeholder community, ensuring scientific publications driven by good publication practice principles.Track and report Scientific Publications performance.Support internal stakeholders (PV, IP/Legal, Regulatory, Research, GMA, etc.) with scientific publications related topics (incl. data transparency and sharing)Manages and is the budget owner of the library tool (ReadCube) as well as subscriptions to journals and info databaseAct as an active member of the Trial Disclosure Team, supporting processes development and implementation with data disclosure, transparency, and sharing.Support planned medical participation at multi-product / disease area congresses, symposia, and events with scientific publication plans and activities.Adherence to existing Policies and Procedures and timely completion of relevant training.


Requirements

A medical degree, Ph.D., or PharmD is preferred; a bachelor's degree in a biomedical discipline or equivalent with experience in publication management is considered≥10 years of experience within medical affairs or clinical research roles (e.g. Publications/Scientific Writing, Medical Information, Medical Communications, Medical Education), 3 years of which include a publications leader role in the pharmaceutical industryExperience in managing vendorsDeep knowledge of scientific publication strategy and planning approaches and good publication practice is requiredFamiliarity with regulatory and legal guidelines regarding publication planning strategy and executionFocus on accountability and ownershipAbility to drive alignment cross-functionally and partner with key internal (incl. GMA, wider Development and Research, HEOR, value strategy & market access, marketing) and external stakeholders (external experts, journals/publishers, vendors, etc.) with a strong customer-focused approachStrong communication, presentation, and writing skillsStrong attention to detailStrong relationship management skillsScientific expertise in the disease/therapeutic area preferredUnquestioned ethicsUnderstanding of the clinical trial design and execution, statistical methods, and clinical trial data reporting requirementsUnderstanding of good publication practices and guidanceFluency in written and spoken English is a prerequisiteExisting right to work in Europe is required


Benefits

Min 80% FTEIdeally on site in Mechelen Belgium or Basel Switzerland or remote with ad hoc travelA balanced salary package based on your capabilities and experience, including extra legal benefits

Vacancy number:24483


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