Associate Director, Medical Communications & Scientific Exchange; MCSE Strategic Execution Lead
Listed on 2026-04-20
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IT/Tech
Medical Imaging
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, 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 humanity.
Learn 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 an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job FunctionMedical Affairs Group
Job Sub FunctionMedical Writing
Job CategoryProfessional
All Job Posting LocationsHorsham, Pennsylvania, United States of America
Job DescriptionJohnson & Johnson Innovative Medicine is recruiting for an Associate Director, Medical Communications & Scientific Exchange (MCSE) Strategic Execution Lead located in Horsham, PA.
About Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science‑based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. 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
Key Responsibilities- Oversee the day‑to‑day operations of the MSL Comms team, including maintenance of trackers and e‑mail distribution lists; communication of important software or training updates; supporting and testing iConnect/CRM functions; and acting as an SME on any platform used by MSL Comms (Veeva iMedical Knowledge and CRM, CURE, etc.)
- Liaise with Janssen Scientific Affairs and colleagues in MISE and JJMC to ensure timely updates to internal systems related to storage and approvals of MSL resources.
- Troubleshoot issues, sometimes urgently, in iMK and CRM in collaboration with the MSL Comms leads.
- Seek continuous improvement and expanded capabilities of iMK and CRM, and other novel approaches to scientific exchange in MCSE.
- Liaise with Learning & Development teams to provide training for MSL onboarding and fill ongoing knowledge gaps regarding optimal usage of iMK and CRM; support training for other MAF staff working with MCSE.
- Oversee operational support for J&J publication review tool, JPUBs.
- Oversee quality assurance of MCSE deliverables.
- Oversee operational support to MCSE Leadership in budgeting activities (SOWs, POs, tracking accruals).
- Work closely with MCSE Leadership to track overall team output and prepare for presentations to senior leadership.
- Support other operational activities in MCSE as required.
- Spearhead digital innovation efforts on behalf of MCSE.
- Gather evidence about current use of digital innovation across US and Global MAF networks, including creation, tracking, and impact of assets.
- Create and implement a plan to trial and expand digital innovation within US IMM MAF.
- Liaise across functions within US IMM MAF, Global IMM MAF, and other Disease Area Strongholds to develop an approach that has broad applicability across J&J.
- Minimum of a Bachelor’s Degree in Life Sciences, Healthcare or related discipline with at least 6 years of medical communications experience or 6 years of related (pharmaceutical) work experience; or an advanced degree (MS, PhD, Pharm
D) with at least 4 years of related (pharmaceutical) work experience. - Demonstrated ability to work in cross‑functional environments and partner with scientists, academicians, clinicians and vendors.
- Experience with process improvement and operations in the pharmaceutical industry.
- Familiarity with Veeva Systems and the Medical/Legal/Regulatory review process.
- Highly proficient in Microsoft PowerPoint, with outstanding slide‑design skills including scientific accuracy, visual appeal, creativity and innovative thinking.
- Detail‑oriented and highly organized.
- Excellent oral and written…
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