Medical Director, Dermatology- US Medical Affairs

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

Medical Director for Dermatology Medical Affairs at Johnson & Johnson, responsible for strategic planning and execution of clinical trials (Phase IIIb & IV, post-marketing, investigator-initiated), serving as a study responsible physician. The role involves protocol development, medical/data monitoring, study operations, data analysis, reporting, writing study reports and publications, and partnering with cross-functional teams on real-world evidence and health economics. The Medical Director will also contribute to regulatory submissions and provide US medical input to R&D.

What you'd actually do

  1. Work with the Dermatology Therapeutic Area Lead, as well as other individuals within Medical Affairs and other functional areas within J&J, as necessary, to facilitate research and expanding the knowledge of J&J products for dermatologic diseases.
  2. Provide subject matter expertise and function as US medical representative with internal stakeholders across multiple functional areas including marketing and sales, health economics and outcomes research, MSLs, and medical information.
  3. Develop and execute Medical Affairs sponsored/supported Phase IIIb/IV trials, registries, real-world evidence, and collaborations by leading study design, protocol development, analysis plan development, and providing overall trial leadership (including execution, monitoring, supervision, compliance, and risk identification/ mitigation). This requires close partnership with a matrixed team inside and outside of Medical Affairs (e.g. Clinical Scientists, Program Management, Biostats, Post-Approval Delivery Unit, Regulatory Affairs, Quality, Medical Monitor, external investigators/Key Opinion Leaders).
  4. Write as well as provide editorial comments for Phase IIIb/IV clinical study reports, abstracts and manuscripts related to J&J supported and sponsored studies.
  5. Contribute to the preparation of regulatory submissions and interactions with Health Authorities (particularly the FDA) and help to ensure regulatory post-marketing commitments are efficiently satisfied with cost-effective, efficient, and scientifically rigorous methods.

Skills

Required

  • Medical expertise in Dermatology
  • Clinical trial design and execution
  • Protocol development
  • Data analysis and interpretation
  • Scientific writing and publications
  • Regulatory affairs knowledge (FDA)
  • Cross-functional collaboration
  • Stakeholder management

Nice to have

  • Real-world evidence generation
  • Health economics and outcomes research
  • Medical Science Liaison (MSL) interaction
  • Payer-related materials development