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Johnson & Johnson

Makes prescription drugs and medical devices

Medical Director - Gastroenterology Therapeutic Area, US Medical Affairs

Biology & BiotechConfirmed live in the last 24 hours
Full-timeHorsham, PA, USANo salary listedHybrid

About the Job

Requirements

  • An MD/DO degree or international equivalent is required.
  • A minimum of 8 years of combined industry, academic, clinical research, or other clinical practice experience is required, including at least 3 years in the pharmaceutical industry and accountability for successful and timely execution of key deliverables.
  • Strong analytical and strategic-thinking aptitude, scientific-writing proficiency, organizational skills, and written and verbal communication skills, including effective scientific oral presentations, are essential.
  • Strong leadership, teaming, and collaboration skills are required, including the ability to work effectively in a matrix environment and participate in and lead cross-functional teams to execute deliverables.
  • Ability to travel up to 20%, primarily domestically with limited international travel.
  • The position follows a hybrid schedule of three office days and up to two remote days per week in Horsham, Pennsylvania.

Responsibilities

  • Develop and execute Medical Affairs-sponsored clinical study programs as Study Responsible Physician, including Phase 3b/4 trials, registries, real-world evidence studies, investigator-initiated studies, and collaborative studies in the Gastroenterology Therapeutic Area.
  • Contribute to or lead study design, protocol development, clinical study reports, and publications; work with matrix clinical trial teams and external investigators and key opinion leaders on study operations; and provide program leadership and medical oversight.
  • Contribute to US Gastroenterology Medical Affairs strategy, including leading one or more Integrated Evidence Teams for approved and pipeline products or indications and working with cross-functional partners to promote and execute strategy, evidence-generation activities, and data-dissemination plans.
  • Contribute to regulatory submissions and interactions with health authorities, particularly the FDA, and help fulfill regulatory post-marketing commitments efficiently and rigorously.
  • Contribute to or lead cross-functional development and maintenance of strategically aligned, annually updated Integrated Evidence Generation Plans for approved and pipeline products or indications, and support payer-related materials and evidence needs for market access.
  • Review and evaluate Investigator-Initiated Study concepts, champion prioritized concepts through review, approval, and funding, and monitor study progress and milestones.
  • Serve as a subject-matter expert on data supporting approved or planned US Immunology gastrointestinal drugs and indications, partnering with marketing brand teams and other commercial and evidence-team partners.
  • Partner with the Gastroenterology Therapeutic Area and groups including Biostatistics, Global Clinical Operations, Regulatory Affairs, Quality Assurance, and Quality Control to create analysis plans, review safety data for database locks, ensure compliance with study monitoring and Standard Operating Procedures and Good Clinical Practice requirements, and support audits as needed.
  • Support medical-information requests from field medical and field commercial teams; support or lead medical-education content development for field medical teams; and partner with medical communications and scientific exchange teams on content development, review, and approval.
  • Contribute to or lead abstracts and manuscripts related to company-supported and sponsored studies, including cumulative or directed safety experience.
  • Develop relationships with inflammatory bowel disease key opinion leaders through clinical-trial development and medical-affairs activities, and establish and foster relationships with medical societies and patient-advocacy organizations.

Desired Qualifications

  • Current or prior Board Certification or Eligibility in Gastroenterology, or experience in research and development or designing and conducting clinical trials, is preferred.
  • Gastroenterology or Immunology Therapeutic Area expertise is preferred.
  • Prior industry or medical-affairs experience, including commercial brand support, medical-launch support, and clinical-study, registry, or real-world evidence study support and execution, is preferred.
  • Prior research and development or other experience with responsibility and accountability for clinical-study planning and execution is a strong asset.
  • People leadership is an asset.

About the Company

Johnson & Johnson

Makes prescription drugs and medical devices

Johnson & Johnson develops prescription medicines and makes medical devices for hospitals, and unlike most big drugmakers, it runs both businesses under one roof. In 2015, its Darzalex became the first antibody drug approved for multiple myeloma, a blood cancer. Its medicines treat cancer, immune diseases such as psoriasis, and mental illnesses such as depression, and patented drugs bring in most of its sales. Its MedTech unit makes heart pumps, catheters that treat irregular heartbeats, surgical sutures, and Acuvue contact lenses. It was founded in 1886 to make sterile surgical dressings, is based in New Brunswick, New Jersey, and spun off its consumer brands, such as Tylenol and Band-Aid, as Kenvue in 2023.

Company size
10,001+
Company stage
IPO
Headquarters
New Brunswick, NJ
Founded
1886

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