Associate Director, Medical Communications & Scientific Exchange (mcse) Strategic Execution Lead

Johnson & Johnson Johnson & Johnson · Pharma · Horsham, PA +1

This role focuses on managing and improving the operational aspects of medical communications and scientific exchange materials within the pharmaceutical industry, with an emphasis on digital innovation and process optimization. It involves overseeing daily operations, liaising with internal and external stakeholders, ensuring quality assurance, and spearheading digital innovation efforts for scientific exchange materials.

What you'd actually do

  1. Oversee the day-to-day operations of MSL Comms team, including but not limited to the 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 of the platforms used by MSL Comms (Veeva iMedical Knowledge and CRM, CURE, etc )
  2. Liaise with Janssen Scientific Affairs (including Medical Content Excellence and colleagues in MISE and JJMC) to ensure timely updates to internal systems related to the storage and approvals of MSL resources
  3. Spearhead digital innovation efforts on behalf of MCSE
  4. Gather evidence about current use of digital innovation across US and Global MAF networks, including creation, tracking, and impact of assets
  5. Create and implement a plan to trial and expand digital innovation within US IMM MAF

Skills

Required

  • Bachelor’s Degree in Life Sciences, Healthcare or related discipline with a minimum of 6 years of medical communications 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
  • 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
  • Must be highly proficient in Microsoft PowerPoint, with outstanding slide design skills with including scientific accuracy, visual appeal, creativity and innovative thinking
  • Detail-orientation and highly organized
  • Excellent oral and written communication skills
  • Excellent time management and organizational skills

Nice to have

  • Experience in Rheumatology, Dermatology, Gastroenterology, Immunology or related therapeutic areas
  • Experience in IT, software, engineering, or related field
  • Experience in pharmaceutical health care compliance environment for external communication of scientific materials, with knowledge of compliant display of scientific data
  • Familiarity with digital medical strategy & communications
  • People management experience is highly preferred, including vendor management experience.

What the JD emphasized

  • Veeva Systems
  • Medical/Legal/Regulatory review process
  • pharmaceutical health care compliance environment