Medical Director Rheumatology - US Medical Affairs

We need to output HTML fragment with sections for headings like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections if posting has real specific content. We must not repeat job title as heading. No Job ID etc. Remove boilerplate like EEO, etc. Must preserve all substantive info. We need to parse the posting. Key sections: - About the role: maybe "Purpose" or description of role. The posting includes "Purpose This role will be a key member...". So we can put that under About the role. - Responsibilities: "You Will Be Responsible For" list of duties. - Requirements / Qualifications: The posting has "Qualifications / Requirements" list. - Skills: maybe "Required Skills Preferred Skills:" list. - Benefits: Not mentioned. No benefits specifics. So omit Benefits. - Pay: Not mentioned. Omit. - Schedule: The posting mentions "Up to 25% travel (primarily domestic & limited international) is required. This position is located in Horsham, PA and follows a hybrid schedule of three days in the office and two days remotely per week." That's schedule info. So we can include Schedule section with that. Also maybe include location? Not required as heading; could be in a short p. We need to preserve all substantive info: include location, hybrid schedule, travel, etc. We must not include boilerplate like EEO, accommodation request, etc. Remove those. We also need to remove duplicated lines. Let's extract content. First paragraph: At Johnson & Johnson... Learn more at jnj.com. As guided by Our Credo... (that's generic corporate fluff). Might be considered boilerplate? It's not specific to role. Might be considered generic but could be kept? The instruction: remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions. The intro about J&J mission might be considered boilerplate but it's not EEO. It's generic corporate description. Might be considered not substantive for the role. Safer to omit? The instruction: "Preserve ALL substantive information; do NOT invent or summarize away detail." The mission statement is not specific to the job; could be considered boilerplate. I'd omit it to keep focused. We need to keep location: Horsham, Pennsylvania, United States of America. We need to keep "Job Function Medical Affairs Group Job Sub Function Medical Affairs Job Category Scientific/Technology" maybe not needed as heading; could be minor metadata folded into short p. We need to keep "About Immunology" section: that's descriptive of the team. Could be part of About the role. We need to keep "Purpose" section. We need to keep "You Will Be Responsible For" list. We need to keep "Qualifications / Requirements" list. We need to keep "Required Skills Preferred Skills:" list. We need to keep schedule/hybrid and travel. Let's craft sections:

About the role

... combine About Immunology and Purpose maybe.

But we need to ensure we don't miss any specifics. Let's extract About Immunology paragraph: "Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses. You can influence where medicine is going by restoring health to millions of people living with immune diseases. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine" That's substantive about the team. Purpose paragraph: "This role will be a key member of the Medical Affairs Rheumatology Therapeutic Area (TA) Team and will report to the Head, Therapeutic Area Lead Rheumatology, US Medical Affairs- Immunology within the broader US Medical Affairs- Immunology organization. They will work closely with the other Rheumatology Medical Directors (and Associate Directors) as well as partners in US and Global Medical Affairs, Real World Value and Evidence (RWV&E), Population Health, Epidemiology, R&D, Biostatistics, and US and Global Commercial Team members supporting Immunology and Rheumatology within the Johnson & Johnson organization to create, shape, influence and drive strategy for Rheumatology pipeline and approved products including evidence generation plans and subsequent execution, ensuring alignment with business objectives and regulatory standards. They will also lead and/or contribute to the development of related abstracts and manuscripts as either an author or reviewer. The Medical Director Rheumatology will partner with other Rheumatology team members in the US and Global Medical Affairs Organization, as well as Real World Value and Evidence (RWV&E), Epidemiology, R&D, biostatistics, commercial Marketing brand, and field based (MSL, commercial, and payer-facing value and evidence) teams. They will shape the clinical and economic value narrative for one or more Rheumatology products/indications by participating in and/or leading their Integrated Evidence Team (IET), accountable for a strong scientific strategy and its execution through evidence generation efforts and their subsequent impactful presentation and dissemination approaches. May also be responsible for leading the strategic development and execution of US Medical Affairs-sponsored and supported clinical studies (Phase IIIb/IV trials, Post-Marketing Requirement studies, and investigator-initiated and collaborative studies) for company products in the Rheumatology TA." That's purpose. We can combine About Immunology and Purpose into About the role. Now Responsibilities: The "You Will Be Responsible For" block is a long paragraph with many duties separated by periods. We need to turn into

• items. Let's parse sentences: - Contribute to US Rheumatology Medical Affairs strategy, by leading one or more approved and pipeline Rheumatology products/indications, Integrated Evidence Teams (IETs), working cross-functionally with partners within the Rheumatology Integrated evidence team (IET), including Medical Science Liaison (MSL) team leaders, Real World Value & Evidence, Field Value & Evidence, Strategic Customer Group, Marketing team brand leads, as well as potentially Rheumatology Disease Area Stronghold (DAS), R&D, Global Medical Affairs and Global Commercial partners to promote and execute the Rheumatology TA Strategy for establishing access as well as plans for and progress and outcomes for evidence generation activities and Data Dissemination Plans. - Contributes to and potentially leads the cross-functional team to develop and maintain a current, strategically aligned and annually updated Integrated Evidence Generation Plan (IEGP) for approved and pipeline Rheumatology products/indications. - And supports payer-related materials and data needs to scientifically support market access efforts. - May develop and execute (as Study Responsible Physician or Scientist [SRP/SRS]) Medical Affairs sponsored clinical study programs, including but not limited to Phase 3b/4 trials, registries, real-world evidence studies, investigator-initiated and/or collaborative studies in the Rheumatology TA. - Contribute/lead study design, protocol development, clinical study report and publication development. - Work closely with the matrix clinical trial teams and external investigators/KOLs on study operations and provide program leadership and medical oversight. - Contribute to the preparation of regulatory submissions and interactions with Health Authorities/FDA and helps to ensure regulatory post-marketing commitments are efficiently satisfied with cost-effective, efficient, and scientifically rigorous methods. - Reviews and evaluates Investigator-Initiated Study (IIS) concepts, champion prioritized concepts through appropriate review, approval, & funding, and monitor study progress/milestones. - Contributes as a subject matter expert on previous and new data in support of US Immunology approved (or planned) drugs and indications, partnering particularly with respective marketing brand teams as well as other commercial and IET partners, including RWVE, SCG, V&E Field, Medical Information & Scientific Communications partners. - Actively partners with individuals in Rheumatology TA and other groups inside and outside Medical Affairs (e.g. Biostats, GCO, Regulatory Affairs, QA and QC) to create Analysis Plans, safety data review for database locks and ensure compliance with study monitoring and other SOP/GCP requirements (and support audits, as needed). - Support the fulfillment of medical information requests from field medical and field commercial teams. - Support/ lead the development of medical education content for field medical team. - Partner with medical communications and scientific exchange teams on content development, review, and approval. - Contributes to or leads the development of abstracts and manuscripts related to J&J supported and sponsored studies, including cumulative and/or directed safety experience. - Identify new key opinion leaders (KOLs) and develop strong KOL collaborations on clinical trial development and medical affairs activities. - Establish and foster relations with medical societies and patient advocacy organizations. We'll make each bullet a
• . Now Qualifications / Requirements: list: - Advanced degree (MD/DO, PhD, PharmD, DNP, etc.) is required. - A minimum of 8 years of combined relevant experience in academic and/or clinical research, clinical practice, and/or pharmaceutical industry with include a history of accountability for key deliverables with demonstration of their timely and successful execution is required. - Experience including commercial brand support, medical launch support experience, and clinical study, registry, or real-word evidence study support and execution are essential. - Prior R&D experience with responsibility and accountability for clinical study planning and execution is an asset. - Rheumatology or Immunology Therapeutic Area expertise is strongly preferred. - Pharmaceutical industry experience is required - Medical affairs experience is highly preferred - Excellent analytical and strategic thinking aptitude, scientific writing proficiency, and strong organizational, written, and verbal communication skills, including proficiency in effective and impactful scientific oral presentations is essential. - Excellent interpersonal and public speaking skills, and experience interacting with health care professionals and other thought leaders is essential - Strong leadership, teaming, and collaboration skills and the ability to work in a matrix environment, collaborating effectively with many cross functional partners and succeed in participating in and leading cross functional teams to execute on deliverables is essential. - Demonstrated commitment to learning emerging technologies, such as AI, through exploration, iteration, and applying new tools over time. - Up to 25% travel (primarily domestic & limited international) is required. - This position is located in Horsham, PA and follows a hybrid schedule of three days in the office and two days remotely per week. Note travel and schedule appear also in Qualifications; but we also have schedule section. We'll keep travel and schedule maybe in Schedule section. But we need to avoid duplication. We'll keep travel and schedule in Schedule section, and not duplicate in Qualifications. However Qualifications includes travel and schedule; we could keep them there but then schedule section would be duplicate. Better to move travel and schedule to Schedule section and remove from Qualifications. But we must preserve all substantive info; we can keep them in Schedule section and not repeat. So we will omit travel and schedule from Qualifications list. Thus Qualifications list will exclude those two items. Now Skills: "Required Skills Preferred Skills: Clinical Research, Collaboration, Data Dissemination, Data Generation, Immunology, Launch Excellence, Medical Affairs, Rheumatology, Stakeholder Collaboration, Strategic Thinking, Strategy Development". This seems like a list of skills. We'll put under Skills section as
  • each. Now we need to include location maybe in a short p under About the role or separate? Could be a short p: "Location: Horsham, PA". But location is already in schedule; we could mention location in schedule section. We'll include location in schedule section. Now we need to ensure we don't include boilerplate like EEO etc. We'll cut those. Now produce HTML fragment:

    About the role

    [combined About Immunology and Purpose text]

    Responsibilities

    • ...
    ...

    Qualifications

    • ...
    ...

    Skills

    • ...
    ...

    Schedule

    Up to 25% travel (primarily domestic & limited international) is