Job Details

ID #51803476
Estado Pennsylvania
Ciudad Springhouse
Full-time
Salario USD TBD TBD
Fuente J&J Family of Companies
Showed 2024-05-30
Fecha 2024-05-30
Fecha tope 2024-07-29
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Associate Director, Global Medical Affairs Publication Operations

Pennsylvania, Springhouse, 19477 Springhouse USA
Aplica ya

Associate Director, Global Medical Affairs Publication Operations - 2406190788WDescriptionJohnson & Johnson Innovative Medicine is currently recruiting for a Associate Director, Global Medical Affairs Publication Operations, to be located in Titusville, NJ, Raritan, NJ; Horsham, PA , Spring House, PA or other Janssen Global Services location in MA.At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com (file:///C:/Users/jamie yacco/AppData/Local/Microsoft/Windows/Temporary Internet Files/Content.Outlook/JHNHJA6O/www.janssen.com) and follow us @JanssenGlobal. Janssen Global Services, LLC is part of the Janssen Pharmaceutical Companies.The Associate Director, Global Medical Affairs Publication Operations will provide expert writing and editing support to ensure timely production of high-quality documents (abstracts, posters, slide presentations, manuscripts, letters to editor, etc.) for publication in medical/scientific journals or presentation at meetings. You will manage and/or review and interpret data and source documents for information required for publication. Assist in table and figure mock-up development. 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.You will also be responsible for scientific publication writing including abstracts, posters/oral presentations and manuscript and be responsible for the overall production of publications and compliance with standard operating procedures/industry standards. You will also assist with updating existing standard operating procedures and publication document guidance as needed.You will also:

Provide direction, oversight and editing for contract medical writers and junior level medical writers.

Assist in updating existing standard operating procedures (SOPs) with respect to writing processes and relevant publication document guidance 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.

QualificationsQualifications

Compensation expectation for range: $118,000-$203,000- A PhD, PharmD, MD or equivalent degree with a minimum of 8 years of relevant pharmaceutical/scientific experience is required OR a Master’s (or other advanced degree) with a minimum of 10 years relevant pharmaceutical/scientific experience is required- Research experience (including compilation of research reports or publications) in academia, the pharmaceutical industry, medical communication agency or as part of a PhD, Pharm.D or postdoctoral program is preferred- CMPP certification is preferred- Demonstrated ability to interpret and organize scientific data is required- The ability to work well independently as well as part of a team is required- Project management experience is preferred- The ability to stay organized, manage time, and work on multiple documents/projects at once is required- Knowledge across several therapeutic areas such as neuroscience, immunology and/or infectious diseases is preferred.

Experience applying AMA, GPP, ICMJE, and similar guidelines is preferred- Experience with medical writing document standards and processes is preferred- Experience using workflow management tool (e.g. PubSTRAT or Datavision) is preferred- Up to 10% travel requiredAt Johnson & Johnson, we’re on a mission to change the trajectory of health for humanity. That starts by creating the world’s healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional, and financial health of our employees and the ones they love. As such, candidates offered employment must show proof of COVID-19 vaccination or secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work.For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com .Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Primary Location NA-US-New Jersey-RaritanOther Locations NA-US-Pennsylvania-Horsham, NA-US-Pennsylvania-Spring House, NA-US-Massachusetts-Raynham, NA-US-New Jersey-TitusvilleOrganization Janssen Global Services, LLC (6085)Job Function Medical WritingReq ID: 2406190788W

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