Job Description

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at .

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Medical Affairs Group

Job Sub Function:

Medical Writing

Job Category:

Professional

All Job Posting Locations:

Horsham Pennsylvania United States of America

Job Description:

Johnson & Johnson US Medical Affairs is recruiting for a Manager Medical Writer located in our Horsham Pennsylvania. This is a hybrid role that will require 3 days in the Horsham office.

We are looking for a Manager Medical Writer to join the Scientific Communications team supporting our Immunology therapeutic area. The writer will support publications (e.g. manuscripts abstracts posters presentations and slide decks) as assigned to develop peer-reviewed publications and congress submissions communicating data from our company-sponsored clinical and observational studies in addition to real-world evidence analyses.

Key Responsibilities :

• Collaborate with Johnson & Johnson US and global stakeholders authors and steering committee members throughout the publication development process. May collaborate with external vendors on projects. Manage correspondence with congress organizers and other personnel.

Medical writing will include but is not limited to:

• Lead writing editing and revising manuscripts abstracts posters and/or presentations. As agreed upon by authors develop all drafts and final submission copies. Additional pub extenders (Plain Language Summaries graphical abstracts etc.) also in scope.

• Provide editorial support for any vendor-assigned congress work or manuscripts to meet timeline expectations. Work closely with SCL and vendor account lead to ensure lead (vendor) writer is supported with data Share Point access and document review.

• Manage working group meetings and collaborate with authors to advance the development of manuscripts/abstracts/posters/presentations.

• Review and interpret data and source documents for information required for publication development. Lead mock-up development of data displays (e.g. tables and figures).

• Identify and resolve with the help of other functional areas clinical and statistical issues in the interpretation of clinical data.

• Conduct detailed literature reviews for topics of interest related to project documents using various repositories.

• Demonstrate mastery of relevant publication 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 other guidelines pertaining to study protocols and clinical study reports.

• May perform other duties as assigned.

Manage assigned writing projects:

• Attend meetings and support assigned therapeutic area(s) publication team(s).

• Manage document development timelines to facilitate timely submission.

• Maintain annotated versions of documents and facilitate review cycles.

• Record/maintain project status using relevant tool(s).

• Shepherd documents through designated review and approval cycles.

• Facilitate collate and adjudicate author and reviewer comments.

• Adjudicate and address quality assurance review.

• Verify completion of mandatory approvals.

• Manage project review/approval in automated workflow system.

• May perform other duties as assigned.

Education:

Required Minimum Education: Bachelors degree or equivalent. Masters PhD or PharmD desirable.

Experience and Skills:

Required Years of Related Experience: Minimum of 5 years of relevant publication writing experience in the pharmaceutical industry.

Required Knowledge Skills and Abilities:

We would value a colleague with these qualities:

• Ability to learn new concepts and recognize how to best interpret summarize and present statistical and medical information to ensure quality and accuracy of content in document types under supervision

• Strong attention to detail

• Strong oral and written communication skills

• Leadership skills both in time management as well as in project/process management

• Able to resolve basic problems independently and complex problems under supervision

• Familiarity with relevant publication industry best practices and publication guidelines

• Learning agility and attention to detail

• Ability to build solid and positive relationships with cross-functional team members

Preferred:

• Microsoft Word Excel Power Point Microsoft Teams SharePoint

• Publications systems experience desired

• ISMPP CMPP or AMWA MWC certification

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 external applicants please contact us via . Internal employees contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

Business Writing Clinical Research and Regulations Clinical Trials Operations Coaching Collaborating Copy Editing Data Synthesis Industry Analysis Medical Affairs Medical Communications Process Improvements Proofreading Quality Validation Standard Operating Procedure (SOP) Tactical Planning Technical Credibility

Required Experience:

Manager

Job Tags

Full time, Work at office, Local area

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