Johnson & Johnson MedTech
Medical Director, Medical Affairs, Johnson & Johnson MedTech
Johnson & Johnson MedTech, Newark, New Jersey, us, 07175
Overview
Medical Director, Medical Affairs, Johnson & Johnson MedTech. This remote role is fully remote in the United States and reports to the Senior Director, Medical Affairs. The position provides medical leadership globally for Johnson & Johnson’s MedTech Endomechanical and Energy Platforms, supporting products across the lifecycle in collaboration with R&D, Global Strategic Marketing, Commercial, and Health Economics and Market Access (HEMA). It includes evidence generation, dissemination activities to support product approvals, claims development, and product adoption, and cross-functional collaboration with medical safety, regulatory, and clinical teams. The role also involves external engagement with key opinion leaders, professional societies, payers, and providers to shape industry insights and portfolio strategies. Responsibilities
Partner with R&D, Clinical Research, Regulatory Affairs, Communications, Legal, Quality & Compliance, Preclinical, HEMA, and Medical Education to lead product development, pre- and post-approval clinical studies, regulatory submissions, downstream claims, safety assessments, and training for the franchise portfolio. Lead generation and dissemination strategies for company-sponsored and investigator-initiated research, including registries. Participate in governance forums and cross-functional teams (Business Unit leadership, product core teams, EGS, portfolio/strategy management, Safety and Quality Review Boards). Engage key opinion leaders, professional societies, payers, and providers to understand care trends and uncover insights to support innovation and portfolio strategy. Provide medical and scientific insights to guide strategy, launches, scientific meetings, and relationships with leading researchers and decision makers. Provide lifecycle medical affairs support, including copy review and medical input for clinical evaluation reports, and medical oversight for materials used in study execution. Collaborate with Medical Safety to review and escalate adverse events from clinical studies as needed. Interpret study outcomes and assist in developing communications and educational strategies for disseminating results. Prepare reports on clinical investigations for regulatory submission and publication to meet evidence requirements for new products and renewals. Contribute to risk management and post-market surveillance activities, including risk mitigation and safety signal detection. Review and approve educational, promotional, and reporting materials for internal stakeholders; prioritize publication proposals with Clinical Science. Align strategy, budget, and resources with cross-functional partners. Attend scientific meetings as an oral presenter and contribute key scientific publications to establish leadership in the field. Safeguard patient safety and participate in environmental scanning, competitive analysis, new product development, and trial coverage as needed. Qualifications
MD/DO with a minimum of 5 years post-graduate medical education experience, including specialty residency, fellowship/subspecialty training, clinical practice, or related research/training. Current medical license preferred. Board Certification and Fellowship in a surgical specialty strongly preferred. Five+ years of attending-level clinical practice preferred. Clinical research experience in medical devices, biologics, or drugs strongly preferred. Experience with global regulatory submissions for medical devices, biologics, or drugs is desirable (PMA/BLA/NDA or global equivalents). Experience in medical safety surveillance and quality improvement activities is desirable. Experience in new product development and partnerships is desirable. Strong leadership, communication, and negotiation skills; ability to build global teams across multiple therapeutic areas is desirable. Demonstrated success in medical data generation, interpretation, and publication is preferred. Experience with natural language processing in research and literature review is desirable. Experience in product risk evaluation and mitigation is preferred. Academic mindset with ability to analyze data to inform clinical trials and innovation is desirable. Additional information
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by law. Reasonable accommodations are available on request during the interview process. The anticipated base pay range for this position is 194000 to 334650. This position is eligible for an annual performance bonus and other company-sponsored benefits as described in the employee benefits summary. For more information on benefits, please visit the Johnson & Johnson careers site.
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Medical Director, Medical Affairs, Johnson & Johnson MedTech. This remote role is fully remote in the United States and reports to the Senior Director, Medical Affairs. The position provides medical leadership globally for Johnson & Johnson’s MedTech Endomechanical and Energy Platforms, supporting products across the lifecycle in collaboration with R&D, Global Strategic Marketing, Commercial, and Health Economics and Market Access (HEMA). It includes evidence generation, dissemination activities to support product approvals, claims development, and product adoption, and cross-functional collaboration with medical safety, regulatory, and clinical teams. The role also involves external engagement with key opinion leaders, professional societies, payers, and providers to shape industry insights and portfolio strategies. Responsibilities
Partner with R&D, Clinical Research, Regulatory Affairs, Communications, Legal, Quality & Compliance, Preclinical, HEMA, and Medical Education to lead product development, pre- and post-approval clinical studies, regulatory submissions, downstream claims, safety assessments, and training for the franchise portfolio. Lead generation and dissemination strategies for company-sponsored and investigator-initiated research, including registries. Participate in governance forums and cross-functional teams (Business Unit leadership, product core teams, EGS, portfolio/strategy management, Safety and Quality Review Boards). Engage key opinion leaders, professional societies, payers, and providers to understand care trends and uncover insights to support innovation and portfolio strategy. Provide medical and scientific insights to guide strategy, launches, scientific meetings, and relationships with leading researchers and decision makers. Provide lifecycle medical affairs support, including copy review and medical input for clinical evaluation reports, and medical oversight for materials used in study execution. Collaborate with Medical Safety to review and escalate adverse events from clinical studies as needed. Interpret study outcomes and assist in developing communications and educational strategies for disseminating results. Prepare reports on clinical investigations for regulatory submission and publication to meet evidence requirements for new products and renewals. Contribute to risk management and post-market surveillance activities, including risk mitigation and safety signal detection. Review and approve educational, promotional, and reporting materials for internal stakeholders; prioritize publication proposals with Clinical Science. Align strategy, budget, and resources with cross-functional partners. Attend scientific meetings as an oral presenter and contribute key scientific publications to establish leadership in the field. Safeguard patient safety and participate in environmental scanning, competitive analysis, new product development, and trial coverage as needed. Qualifications
MD/DO with a minimum of 5 years post-graduate medical education experience, including specialty residency, fellowship/subspecialty training, clinical practice, or related research/training. Current medical license preferred. Board Certification and Fellowship in a surgical specialty strongly preferred. Five+ years of attending-level clinical practice preferred. Clinical research experience in medical devices, biologics, or drugs strongly preferred. Experience with global regulatory submissions for medical devices, biologics, or drugs is desirable (PMA/BLA/NDA or global equivalents). Experience in medical safety surveillance and quality improvement activities is desirable. Experience in new product development and partnerships is desirable. Strong leadership, communication, and negotiation skills; ability to build global teams across multiple therapeutic areas is desirable. Demonstrated success in medical data generation, interpretation, and publication is preferred. Experience with natural language processing in research and literature review is desirable. Experience in product risk evaluation and mitigation is preferred. Academic mindset with ability to analyze data to inform clinical trials and innovation is desirable. Additional information
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by law. Reasonable accommodations are available on request during the interview process. The anticipated base pay range for this position is 194000 to 334650. This position is eligible for an annual performance bonus and other company-sponsored benefits as described in the employee benefits summary. For more information on benefits, please visit the Johnson & Johnson careers site.
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