Johnson & Johnson MedTech
Medical Director, Medical Affairs, Johnson & Johnson MedTech
Johnson & Johnson MedTech, Kansas City, Kansas, United States, 66115
Overview
Medical Director, Medical Affairs, Johnson & Johnson MedTech. This fully remote role in the United States reports to the Senior Director, Medical Affairs and provides medical leadership globally to Johnson & Johnson MedTech Endomechanical and Energy Platforms. The role supports products across the lifecycle in collaboration with R&D, Global Strategic Marketing, Commercial, and Health Economics and Market Access (HEMA). It drives evidence generation and dissemination activities to support product approvals, claims development, and product adoption. Job Description
Johnson and Johnson Family is recruiting a Medical Director, Medical Affairs, Johnson & Johnson MedTech. This role is Fully Remote in the United States. This is a remote role available in the Continental US; candidates from any location across the country may apply. Key responsibilities include working with cross-functional teams to provide medical leadership for product development, pre- and post-approval clinical studies, regulatory submissions, downstream claims, safety assessments, and product launches. The role involves governance participation, engagement with Key Opinion Leaders and professional societies, and development of medical education and training materials. It also includes safeguarding patient safety and contributing to risk management, scientific dissemination, and publication activities. Responsibilities
Collaborate with R&D, Clinical Research, Regulatory Affairs, Communications, Legal, Quality & Compliance, Preclinical, Health Economics & Market Access, and Professional Medical Education to lead product development, clinical studies, regulatory submissions, and training for key products. Develop and execute product and procedural evidence generation and dissemination strategies for company-sponsored and investigator-initiated research, including registries. Participate in governance forums and cross-functional teams (Business Unit, product core teams, Safety and Quality Review Boards). Engage Key Opinion Leaders, Professional Societies, Payers and Providers to understand trends and inform portfolio strategies. Provide medical and scientific insights to guide strategic direction, product launches, scientific meetings, and stakeholder relationships. Provide lifecycle medical affairs support (e.g., copy review, medical information requests, input into clinical evaluation reports). Oversee development of materials for study execution (investigator brochures, training materials). Collaborate with Medical Safety to review and escalate adverse events from clinical studies. Interpret study outcomes and assist in communicating results through education strategies. Prepare reports on clinical investigations for regulatory submissions and publications to meet evidence requirements. Contribute to medical input for risk management and post-launch surveillance. Review and approve educational, promotional, and reporting materials for internal stakeholders; prioritize publications with Clinical Science. Align strategy, budget, and resources with cross-functional partners. Attend key scientific meetings, present as needed, and publish key findings to establish expertise in the field. Safeguard patient safety and conduct environmental scanning, competitive analysis, and product development activities as appropriate. Qualifications
MD/DO with at least 5 years of relevant post-graduate medical education and experience (residency, fellowship, subspecialty training, clinical practice, research, or related). Current medical license preferred. Board Certification and Fellowship in a surgical specialty strongly preferred. Five or more years of clinical practice as an attending-level physician preferred. Clinical research experience in medical devices, biologics, or drugs strongly preferred. Experience supporting global regulatory submissions for medical devices, biologics, or drugs desirable (PMA/BLA/NDA or global counterparts). Experience in medical safety surveillance and quality improvement activities desirable. Experience in new product development and cross-functional partnerships desirable. Strong leadership and relationship-building skills; strong communication and negotiation abilities. Ability to build and lead global teams across different clinical specialties; experience with medical data generation, interpretation, and publication preferred. Experience with natural language processing in research and literature review desirable. Experience in product risk evaluation and mitigation desirable. Academic mindset with ability to analyze data to inform clinical trial decisions; ability to review literature to support innovation. Additional Information
Equal Opportunity Employer. All qualified applicants will receive consideration 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 available upon request. The anticipated base pay range for this position is 194000 to 334650. This position may be eligible for an annual performance bonus. Benefits include medical, dental, vision, life insurance, disability coverage, retirement plans, and paid time off as described by company policy.
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Medical Director, Medical Affairs, Johnson & Johnson MedTech. This fully remote role in the United States reports to the Senior Director, Medical Affairs and provides medical leadership globally to Johnson & Johnson MedTech Endomechanical and Energy Platforms. The role supports products across the lifecycle in collaboration with R&D, Global Strategic Marketing, Commercial, and Health Economics and Market Access (HEMA). It drives evidence generation and dissemination activities to support product approvals, claims development, and product adoption. Job Description
Johnson and Johnson Family is recruiting a Medical Director, Medical Affairs, Johnson & Johnson MedTech. This role is Fully Remote in the United States. This is a remote role available in the Continental US; candidates from any location across the country may apply. Key responsibilities include working with cross-functional teams to provide medical leadership for product development, pre- and post-approval clinical studies, regulatory submissions, downstream claims, safety assessments, and product launches. The role involves governance participation, engagement with Key Opinion Leaders and professional societies, and development of medical education and training materials. It also includes safeguarding patient safety and contributing to risk management, scientific dissemination, and publication activities. Responsibilities
Collaborate with R&D, Clinical Research, Regulatory Affairs, Communications, Legal, Quality & Compliance, Preclinical, Health Economics & Market Access, and Professional Medical Education to lead product development, clinical studies, regulatory submissions, and training for key products. Develop and execute product and procedural evidence generation and dissemination strategies for company-sponsored and investigator-initiated research, including registries. Participate in governance forums and cross-functional teams (Business Unit, product core teams, Safety and Quality Review Boards). Engage Key Opinion Leaders, Professional Societies, Payers and Providers to understand trends and inform portfolio strategies. Provide medical and scientific insights to guide strategic direction, product launches, scientific meetings, and stakeholder relationships. Provide lifecycle medical affairs support (e.g., copy review, medical information requests, input into clinical evaluation reports). Oversee development of materials for study execution (investigator brochures, training materials). Collaborate with Medical Safety to review and escalate adverse events from clinical studies. Interpret study outcomes and assist in communicating results through education strategies. Prepare reports on clinical investigations for regulatory submissions and publications to meet evidence requirements. Contribute to medical input for risk management and post-launch surveillance. Review and approve educational, promotional, and reporting materials for internal stakeholders; prioritize publications with Clinical Science. Align strategy, budget, and resources with cross-functional partners. Attend key scientific meetings, present as needed, and publish key findings to establish expertise in the field. Safeguard patient safety and conduct environmental scanning, competitive analysis, and product development activities as appropriate. Qualifications
MD/DO with at least 5 years of relevant post-graduate medical education and experience (residency, fellowship, subspecialty training, clinical practice, research, or related). Current medical license preferred. Board Certification and Fellowship in a surgical specialty strongly preferred. Five or more years of clinical practice as an attending-level physician preferred. Clinical research experience in medical devices, biologics, or drugs strongly preferred. Experience supporting global regulatory submissions for medical devices, biologics, or drugs desirable (PMA/BLA/NDA or global counterparts). Experience in medical safety surveillance and quality improvement activities desirable. Experience in new product development and cross-functional partnerships desirable. Strong leadership and relationship-building skills; strong communication and negotiation abilities. Ability to build and lead global teams across different clinical specialties; experience with medical data generation, interpretation, and publication preferred. Experience with natural language processing in research and literature review desirable. Experience in product risk evaluation and mitigation desirable. Academic mindset with ability to analyze data to inform clinical trial decisions; ability to review literature to support innovation. Additional Information
Equal Opportunity Employer. All qualified applicants will receive consideration 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 available upon request. The anticipated base pay range for this position is 194000 to 334650. This position may be eligible for an annual performance bonus. Benefits include medical, dental, vision, life insurance, disability coverage, retirement plans, and paid time off as described by company policy.
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