Associate Medical Director, US Medical Affairs, Dermatology
Johnson & Johnson
June 27, 2026
Remote friendly (Horsham, PA)
United States
Medical Affairs
Associate Medical Director, US Medical Affairs, Dermatology (Horsham, PA)
Purpose
- Lead development and execution of Medical Affairs sponsored/supported clinical programs for Dermatology products.
- Formulate and execute scientific strategy for marketed and pipeline products.
- Address medical questions and educational gaps from field insights and Dermatology HCPs.
- Lead or contribute to abstracts and manuscripts as author or reviewer.
You Will Be Responsible For
- Contribute to US Dermatology Medical Affairs strategy; support integrated evidence teams (IETs) for approved/pipeline indications.
- Develop and maintain an Integrated Evidence Generation Plan (IEGP) for Dermatology products/indications.
- Support payer-related materials/data for market access.
- Serve as subject matter expert analyzing key US Immunology data for therapies/indications.
- Develop abstracts/manuscripts focused on efficacy, outcomes, and safety/adverse events.
- Serve as Study Responsible Physician/Scientist (SRP/SRS) and oversee study design, protocol development, regulatory communications, investigator interactions, and execution for studies (Phase IIIb/IV, registries, real world evidence, investigator-initiated).
- Partner cross-functionally (Biostats, GCO, Regulatory, QA/QC) on Analysis Plans, safety review, database lock support, compliance with SOP/GCP; support audits.
- Prepare regulatory submissions and interact with Health Authorities (US FDA); ensure post-marketing commitments.
- Build/manages relationships with key opinion leaders and investigators.
Qualifications / Requirements
- Bachelor’s required; PharmD/PhD/MD/DO preferred (NP/PA considered).
- 1.5+ years pharma industry preferred and/or 5+ years post-graduate clinical practice (may include research).
- Strong communication (oral presentations), organizational, and time-management skills.
- Ability to work in a matrix and lead cross-functional teams.
- Proficiency in English.
Preferred
- Experience in dermatology.
- Experience planning/executing/writing regulatory submissions, protocols, and/or scientific manuscripts.
- Experience with data analysis/review and/or clinical study execution (investigator/medical monitor/clinical scientist).
- Experience with clinical use/study of immunologic biologics and small molecules.
Other
- 10%–20% annual travel (primarily domestic).
- Hybrid: 3 days office, 2 days remote per week.
Purpose
- Lead development and execution of Medical Affairs sponsored/supported clinical programs for Dermatology products.
- Formulate and execute scientific strategy for marketed and pipeline products.
- Address medical questions and educational gaps from field insights and Dermatology HCPs.
- Lead or contribute to abstracts and manuscripts as author or reviewer.
You Will Be Responsible For
- Contribute to US Dermatology Medical Affairs strategy; support integrated evidence teams (IETs) for approved/pipeline indications.
- Develop and maintain an Integrated Evidence Generation Plan (IEGP) for Dermatology products/indications.
- Support payer-related materials/data for market access.
- Serve as subject matter expert analyzing key US Immunology data for therapies/indications.
- Develop abstracts/manuscripts focused on efficacy, outcomes, and safety/adverse events.
- Serve as Study Responsible Physician/Scientist (SRP/SRS) and oversee study design, protocol development, regulatory communications, investigator interactions, and execution for studies (Phase IIIb/IV, registries, real world evidence, investigator-initiated).
- Partner cross-functionally (Biostats, GCO, Regulatory, QA/QC) on Analysis Plans, safety review, database lock support, compliance with SOP/GCP; support audits.
- Prepare regulatory submissions and interact with Health Authorities (US FDA); ensure post-marketing commitments.
- Build/manages relationships with key opinion leaders and investigators.
Qualifications / Requirements
- Bachelor’s required; PharmD/PhD/MD/DO preferred (NP/PA considered).
- 1.5+ years pharma industry preferred and/or 5+ years post-graduate clinical practice (may include research).
- Strong communication (oral presentations), organizational, and time-management skills.
- Ability to work in a matrix and lead cross-functional teams.
- Proficiency in English.
Preferred
- Experience in dermatology.
- Experience planning/executing/writing regulatory submissions, protocols, and/or scientific manuscripts.
- Experience with data analysis/review and/or clinical study execution (investigator/medical monitor/clinical scientist).
- Experience with clinical use/study of immunologic biologics and small molecules.
Other
- 10%–20% annual travel (primarily domestic).
- Hybrid: 3 days office, 2 days remote per week.