Publication Manager, Global Medical Affairs (Autoantibody)

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Job Function:
Medical Affairs Group

Job Sub Function:
Medical Writing

Job Category:
People Leader

All Job Posting Locations:
Horsham, Pennsylvania, United States of America

:

We are searching for the best talent for Publication Manager, Global Medical Affairs (Autoantibody) located in Horsham, PA.

About Immunology

Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses. You can influence where medicine is going by restoring health to millions of people living with immune diseases.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at

The Publication Manager, Global Medical Affairs (Autoantibody) will lead multiple processes related to the dissemination of key strategic publications, providing key operational support, project management, and proactive planning. The individual will play an integral role in the successful execution of Global Publication Plans across multiple assets across the Autoantibody therapeutic area (which includes autoimmune neurology, rheumatology, hematology, and maternal-fetal immunology).

Key Responsibilities:

• Assist Scientific Communications Lead (SCL) with development, execution, and maintenance of the Global Strategic Publication Plan for Autoantibody, which includes indication-specific and cross-therapeutic area publication plans integrated over multiple functions and teams.
• Coordinate, track, and summarize publication status and due dates from multiple vendors, internal publication team members, cross-functional team members (eg Market Access, Translational), and regional team members to assure accurate updates to publication plans.
• Assist with planning, content development, and execution of Strategic Publication Team (SPT) meetings (~1-2 per month)
• Liaise with multiple vendors, publication team members, cross-functional, and regional teams to develop/update Publication Plan decks, collate publication metrics, develop/update bibliographies, or develop/maintain other centralized resources for broad team usage.
• Assist SCL with vendor management, projected timelines, tracking, metrics, and budget (planning and accruals)
• Lead the internal dissemination of final scientific publication materials, publication plans, and congress submissions/disposition/presentation summaries.
• Provide direction and training when needed to cross-functional and regional partners on SOPs, work instructions, and systems required for execution of publications (eg, JPUBS, presentation templates, encores)
• Attend scientific congresses and meet with external authors to discuss planning and logistics of publications
• Organize and maintain repositories of final abstracts, posters, orals, and manuscripts for ease of reference for global and regional partners. Partner with publication vendors to assure documentation for abstracts, posters, and manuscripts.

Requirements:

Education:

• BA/BS required

Required:

• A minimum of 5 years of combined relevant experience in the pharmaceutical industry is required.
• Excellent oral and written communication, presentation skills, and project management skills are required
• Strong proficiency with MS office platforms
• Strong communication skills and the ability to prioritize assignments
• Critical thinking, intellectual curiosity, and team building skills
• Up to 10% travel; some travel may be international
• This position is located in Horsham, PA and follows a hybrid schedule of three days in the office and up to two days remote per week.

Preferred:

• Prior experience in a publication-focused Medical Affairs or Publications Manager role (or agency equivalent) for 2 or more years is strongly preferred
• A demonstrated track record of success within Medical Affairs, clinical environment, and/or scientific functions is desired
• Familiarity with external publication guidelines (GPP, ICMJE, AMA, etc), CMPP credentials, and/or industry-specific publication best practices/SOPs encouraged

Johnson & Johnson is an 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, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via or contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:
Analytics Insights, Business Writing, Clinical Research and Regulations, Clinical Trials Operations, Copy Editing, Cross-Functional Collaboration, Developing Others, Inclusive Leadership, Industry Analysis, Leadership, Medical Affairs, Medical Communications, Performance Measurement, Quality Validation, Standard Operating Procedure (SOP), Tactical Planning, Team Management