Medical Director, Spine

Medical Director Orthopaedics, SpineDePuy Synthes, part of the Johnson & Johnson Medical Devices Companies is recruiting for a Medical Director Orthopaedics, Spine to be based in one of the following facility locations in Raynham MA, West Chester PA, Warsaw IN, or Palm Beach Gardens FL. This is a part-time role anticipating a minimum of 3 days per week, allowing 1-2 days per week of external clinical practice. The preferred arrangement is for this role is hybrid remote to be based at one of the locations listed above; however, remote work with periodic travel to one of the locations may be considered on a case-by-case basis in certain circumstances for East Coast candidates.About OrthopaedicsFueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.Are you passionate about improving and expanding the possibilities of Orthopaedics? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma; craniomaxillofacial; sports, extremities, and foot and ankle; spine; and robotics and digital surgery. Your unique talents will help patients on their journey to wellness.This role provides medical affairs support within the spine platform. Leading with both outside-to-inside vision to assimilate opportunities of unmet patient and provider needs, and inside-to-outside vision to communicate the medical, surgical, and scientific this role provides strategic input to inform the innovative agenda within the Platform Portfolio. This role provides medical input throughout product development and life-cycle management, including management of regulatory documents, critical evaluation of clinical risk and input regarding potential patient safety issues. This role collaborates cross-functionally to support product development, including evidence generation and dissemination to drive market registration, access and adoption. This role supports medical education to internal and external stakeholders, and commercialization activities to drive market adoption.Tasks/Duties/ResponsibilitiesINSIGHT MANAGEMENT AND BUSINESS DEVELOPMENT SUPPORT (15%)Engage with omni-channel external sources of information (key opinion leaders, medical societies, literature, social media, etc.) to capture, assess, and translate opportunities of unmet patient and provider needs and trends in the medical/healthcare ecosystems.Support business leaders by providing medical and scientific expertise and omni-channel insights to help shape optimal business development strategy and targets, including product launches, key scientific meetings, relationship management with leading research physicians, critical evaluation of current literature and competitive activity, and in other domains where medical and scientific expertise is required.Validate Target Product Profiles across the assigned innovation pipeline, including gathering and assimilating input from Medical Affairs leaders across key markets.Provide strategic medical support for operating companies with no dedicated medical affairs personnel (and as requested for those companies with medical teams) including to help drive global innovation agenda through leadership and partnership with the Innovation leaders: Global Strategic Marketing, New Business Development, R&D, Regulatory, Clinical, Quality, & Supply Chain leveraging deep medical expertise.INTERNAL PROCESS SUPPORT (50%)Work with cross-functional partners, including but not limited to R&D, Clinical Affairs, Regulatory Affairs, Health Economics & Market Access (HEMA) and Marketing to provide leadership with product development and commercial plans to support product launch, training content and delivery.Provide medical/surgical/scientific insights into design requirements, concept and prototype testing.Provide input into risk management processes for hazard/harm identification & risk mitigation.Assess device performance, including clinical benefits and safety profile, to evaluate the appropriate Risk-Benefit balance to support market registration and throughout life cycle.Work with Medical Safety and Post-Market Surveillance to assess, analysis and interpret events, complaints, signals and trends from clinical studies, literature, complaints, etc.Provide medical/surgical/scientific support for external regulatory inspections and audits, and internal audits.Provide expertise to support addressing complex medical information requests.Provide physician perspective, advice, guidance, and expertise as a medical expert for non-MD colleagues in medical affairs in matters requiring escalation or medical consultation.Provide expert medical/surgical/scientific support to Professional Education, Communications, Legal/HCC, HR Communications.EVIDENCE GENERATION SUPPORT (15%)Assist medical evidence generation leaders to develop and execute global strategies for evidence generation for new and existing products, including medical interpretation of clinical analyses, and in the review and approval of clinical study reports and scientific articles (abstracts, manuscripts, etc), in order to support regulatory approval/clearance, health technology assessment, customer access, medical safety and post-marketing support.LIFE CYCLE MANAGEMENT (LCM) SUPPORT (15%)Provide Lifecycle Management for marketed products including labelling updates, medical support and accountability for technical files and documents and medical support to Quality groups.Research, prepare and document responses to Medical Information Requests from Healthcare providers; review and approve medical content in Copy Approval process; and consults with Franchise Medical Director when needed.S/he will provide consultation in support of literature review, analysis and conclusions for Clinical Evaluation Reports (CER) and provide review of CERs and assists in preparation of periodic safety reports for assigned products.Assist in reviewing of risk evaluation (PRE or PRA) documents.Required education, credentials and experienceRequired Minimum Education is a MD or equivalentCompletion of an accredited orthopedic surgery or neurological surgery residency and a minimum 1-year fellowship in spine surgery (or equivalent spine surgical training) is required.Candidate must have a minimum of 5 years relevant experience (beyond initial licensure) including clinical practice, dedicated research, or other related training/experience.Qualifications continued:Previous experience leading in medical affairs, clinical development, or related roles in research / medical device industry is highly beneficial.Strong understanding of clinical trends and the related healthcare market environment, with deep connections in the digital-, med tech- ecosystem is required.Background and medical expertise in assessment of clinical risk-benefit throughout product development and life-cycle management, with deep knowledge and understanding of all applicable standards / regulations requiring medical input, such as risk management, complaint management, reporting requirements, etc. is required.Ability to be strong advocate for patient-centric decision making is essential.Demonstrated ability to build successful relationships & develop partnerships with key business stakeholders & externally with regulators, investigators, etc. is crucially important.Strong business acumen is essentialThe ability and willingness to travel approximately 15% Domestic and International. The travel estimate would be greater (~30%) for talent who is not based at one of the previously mentioned locations.The anticipated base pay range for this position is $204,000 - $351,900Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone Orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes, and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.Johnson & Johnson is an Affirmative Action and 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