Impactful Associate Medical Director, Dermatology & Respiratory

Johnson Johnson; Spring House (PA); Hybrid; USD 159,000 - 275,000; Full time

Job summary

Johnson & Johnson is seeking an Associate Medical Director, Dermatology and Respiratory, to join the Clinical Development organization in Spring House, PA (hybrid consideration possible across US locations). This physician-lead role focuses on late-stage dermatology and immune-mediated diseases, driving trial design, safety oversight, data interpretation, and regulatory deliverables.

You will collaborate with clinical scientists and matrix partners, author abstracts and manuscripts, and

Qualifications

• MD or equivalent medical degree required.
• Board Certification/Eligibility in dermatology, allergy and immunology, or pulmonary desirable.
• Experience in immune-mediated dermatology/allergy/immunology/pulmonary diseases preferred.
• Experience in design, execution, and reporting of interventional clinical trials desired.

Responsibilities

• Contribute to Phase 2/3 dermatology and respiratory trials, aligned with development strategy and GCP.
• Provide medical oversight including safety review and data interpretation.
• Collaborate with cross-functional teams to drive study milestones and regulatory deliverables.
• Develop and review study concepts, protocols, and regulatory documents.
• Contribute to regulatory submissions and health authority interactions.
• Lead scientific writing and publications from trial data.

Skills

Clinical development

Regulatory knowledge

Medical writing

Cross-functional collaboration

Education

MD or equivalent medical degree

Board Certification/Eligibility in dermatology/allergy/immunology/pulmonary

Job description

Johnson & Johnson is seeking an Associate Medical Director, Dermatology and Respiratory, to join the Clinical Development organization in Spring House, PA (hybrid consideration possible across US locations). This physician-lead role focuses on late-stage dermatology and immune-mediated diseases, driving trial design, safety oversight, data interpretation, and regulatory deliverables.

You will collaborate with clinical scientists and matrix partners, author abstracts and manuscripts, and