Medical Director, Medical Affairs, Johnson & Johnson Medtech

7+ years

Not Disclosed

Remote, USA

10 Nov. 5, 2024

Job Description

Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Medical Director, Medical Affairs, Johnson & Johnson MedTech

Function: Medical Affairs Group
Sub-function: Medical Affairs
Location: Cincinnati, Ohio, United States
Date Posted: October 29, 2024
Requisition Number: 2406218143W

About Johnson & Johnson:

At Johnson & Johnson, we believe health is everything. For over 130 years, we’ve been at the forefront of healthcare innovation, improving lives through smarter, less invasive treatments and personalized solutions. Our expertise spans Innovative Medicine and MedTech, uniquely positioning us to address the world’s most complex health challenges. As part of the Johnson & Johnson Family of Companies, we are dedicated to building a healthier world for humanity. Learn more at www.jnj.com.

We embrace a culture where diversity, equity, and inclusion (DEI) are central to our mission, fueling innovation and helping us serve the diverse needs of communities around the globe. At Johnson & Johnson, everyone belongs, and we are committed to creating an inclusive, welcoming environment for all.

Position Overview:

Johnson & Johnson MedTech is seeking a dynamic Medical Director for Medical Affairs, based in Cincinnati, Ohio. This critical leadership role will focus on providing medical expertise and strategic oversight across the Endomechanical and Energy Platforms of Johnson & Johnson MedTech.

In this position, the Medical Director will work closely with R&D, Global Strategic Marketing, Clinical Research, Regulatory Affairs, and Health Economics & Market Access (HEMA) to provide medical leadership throughout the product lifecycle. You will collaborate across functions to support product approvals, evidence generation, claims development, and the successful adoption of medical technologies.

This role will also focus on global medical affairs strategy, engaging with Key Opinion Leaders (KOLs), surgeons, regulatory agencies, and professional societies to shape the industry landscape, identify unmet medical needs, and ensure our products align with the evolving standards of care.

Key Responsibilities:

Global Medical Leadership:
Provide leadership for MedTech Endomechanical and Energy Platforms, supporting the entire product lifecycle from R&D to commercialization. Collaborate across functions to ensure alignment with medical strategy and business objectives.
Evidence Generation & Dissemination:
Work with Clinical Research to drive evidence generation activities that support product approval, regulatory submission, claims development, and product adoption. Lead investigator-initiated research, registries, and other medical research initiatives to ensure robust scientific evidence.
Product Development Support:
Partner with R&D and Regulatory Affairs to provide medical oversight during product development and clinical trials. Contribute to the preparation of clinical investigation reports and regulatory submissions for new products.
Stakeholder Engagement:
Build and maintain strong relationships with KOLs, surgeons, regulatory agencies, and professional societies. Work closely with these stakeholders to identify clinical trends, unmet needs, and future opportunities for innovation.
Medical Strategy & Portfolio Support:
Contribute to the development of long-term product portfolio strategies. Provide scientific input into strategic marketing plans, product launches, and business development opportunities.
Training & Education:
Lead the development of educational programs for both internal and external stakeholders. Ensure that the commercial and clinical teams are well-equipped with up-to-date scientific and clinical data to support product positioning and market adoption.
Medical Oversight & Compliance:
Oversee the creation and approval of medical communications, training materials, and educational resources. Ensure compliance with regulatory standards and company policies.
Risk Management:
Collaborate with the Medical Safety team to monitor and assess adverse events and product safety throughout the product lifecycle. Provide medical oversight for risk management plans and post-market surveillance activities.

Qualifications:

Required:

MD/DO degree or equivalent with at least 5 years of relevant experience in post-graduate medical education (specialty residency, fellowship, clinical practice, research, etc.).
Strong background in clinical practice, particularly within a surgical specialty. Board certification and fellowship training in a surgical specialty is strongly preferred.
5+ years of clinical experience, ideally in medical device or biologics sectors.
Demonstrated experience in clinical research, regulatory submissions, and medical safety monitoring (preferably for medical devices or biologics).
Proven ability to lead cross-functional teams, work with senior leadership, and engage external stakeholders (e.g., KOLs, surgeons, regulatory agencies).
Strong communication and negotiation skills, with the ability to influence both internal and external partners.
Experience in evidence generation, data analysis, and publication in medical/scientific journals.
Ability to work in a global environment, managing multiple priorities across diverse teams and business units.

Preferred:

Experience with medical device development, clinical trial design, and regulatory processes.
Familiarity with natural language processing and its applications in research and literature review.
Proven track record in risk management and product lifecycle management.

Why Join Us?

At Johnson & Johnson, we are committed to supporting your career development, well-being, and personal growth. We offer a competitive compensation package, including performance bonuses, and a comprehensive range of benefits such as medical, dental, and vision insurance, 401(k) retirement plan, vacation and paid time off.

This is your chance to be part of a leading company that is shaping the future of MedTech innovation. By joining our team, you’ll have the opportunity to contribute to meaningful change in the medical device industry and make a lasting impact on the lives of patients worldwide.

Diversity, Equity & Inclusion at Johnson & Johnson:

We are 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, or protected veteran status. We are committed to creating an inclusive environment where all individuals feel they belong and can thrive.

For more information about our employee benefits and wellness programs, please visit www.careers.jnj.com.

Ready to Apply?
If you are a strategic leader with a passion for advancing healthcare through MedTech innovation, apply today for the Medical Director, Medical Affairs role at Johnson & Johnson MedTech!

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Medical Director, Medical Affairs, Johnson & Johnson Medtech

Job Description

Medical Director, Medical Affairs, Johnson & Johnson MedTech

About Johnson & Johnson:

Position Overview:

Key Responsibilities:

Qualifications:

Why Join Us?

Diversity, Equity & Inclusion at Johnson & Johnson:

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