Johnson & Johnson Innovative Medicine is recruiting for an Associate Director, MSL Communications (Immunology), to be based in Horsham, Pennsylvania.

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential. At Johnson & Johnson, we all belong.

• Create and maintain scientific communication materials as needed to support the U.S. Immunology MSL organization
• Project management of communication materials (e.g. lead prioritization meetings and track prioritization, timelines and progress for communication materials including MSL proactive and reactive slide decks)
• Support slide creation and formatting from abstracts from medical congresses and other clinical/scientific meetings for development of post-congress medical information request decks
• Oversee quality control to ensure scientific accuracy of reactive decks and facilitate their review and approval process
• In collaboration with Medical Affairs colleagues, collect and critically analyze pertinent internal and external documents and studies that provide scientific rationale for the use of J&J products
• Support the development and review of, and approval process for, compliant materials for proactive usage by MSLs
• Collaborate with MSL partners for additional ad hoc communication material needs
• Management of, i.e. provide direction, oversight, and feedback to, contractor(s) and vendor(s)
• Track and analyze metrics of communication material use by MSLs
• Facilitate troubleshooting of communication material access, formatting, and function between desktop and tablet
• Develop and maintain effective working relationships with internal stakeholders (e.g., MSLs, MSL Head & Field Directors, Medical Directors, Medical Communications & Scientific Exchange, Integrated Evidence Team Leads) to fully understand in the strategic scientific needs and identify how the Associate Director, MSL Communications can meet such needs through development of specific field Medical Affairs tools and resources

• A minimum of a Bachelor's Degree in Life Sciences, Healthcare or related discipline with a minimum of 6 years of medical communications or medical writing experience or 6 years of related (pharmaceutical) work experience or an advanced degree (MS, PhD, PharmD) discipline with a minimum of 4 years related (pharmaceutical) work experience is required

• Demonstrated ability to work in cross-functional environments as well as ability to partner with scientists, academicians, clinicians and vendors is required
• Must be highly proficient in Microsoft PowerPoint, with outstanding slide design skills with including scientific accuracy, visual appeal, creativity and innovative thinking
• Ability to translate complex clinical concepts into simple, digestible and appealing visual displays is required
• Detail-orientation with ability to efficiently fact-check and find errors is required
• Excellent oral and written communication skills are required
• Excellent time management and organizational skills are required
• Experience in Word, Microsoft Office, Excel, and Adobe Professional is required

• Experience in Rheumatology, Dermatology, Gastroenterology, Immunology or related therapeutic areas is highly preferred
• Experience in pharmaceutical health care compliance environment for external communication of scientific materials, with knowledge of compliant display of scientific data is highly preferred
• People management experience is highly preferred, including specifically contractor and vendor management experience
• Familiarity with Veeva Systems or the Medical/Legal/Regulatory review process is preferred