Director, Medical Affairs (OTTAVA Surgical Robotics)

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:

Medical Affairs Group

Job Sub Function:

Medical Affairs – MD

Job Category:

Scientific/Technology

All Job Posting Locations:

Cincinnati, Ohio, United States of America, Santa Clara, California, United States of America

Job Description:

We are searching for the best talent for a Director, Medical Affairs (OTTAVA Surgical Robotics).  This position can be located within a commutable distance of either Santa Clara, CA or Cincinnati, OH and will be fully on-site.  Relocation assistance is available to qualified candidates.

Purpose: The Director, Medical Affairs (OTTAVA Surgical Robotics) is responsible for co-leading the development and implementation of innovative surgical robotic systems. This role involves overseeing clinical research, ensuring compliance with medical regulations, supporting medical safety, and guiding the integration of advanced technologies into surgical practices. The candidate must possess a strong background in medicine and technology, coupled with leadership experience in managing multidisciplinary teams.

Key responsibilities include strategic planning, collaboration with engineering and research teams, supporting medical safety documentation, and maintaining a focus on improving patient outcomes through technological advancements. The role demands excellent communication skills for liaising with healthcare professionals, regulatory bodies, and industry partners. This position is pivotal in shaping the future of surgical procedures and requires a visionary approach to healthcare technology.

You will be responsible for:

Strategic Leadership and Vision

• Collaborate in the development and articulation of a clear vision for the integration of MIS/Surgical Robotics into healthcare systems. Assist in the formulation and execution long-term strategic plans and objectives for the surgical robotics division.
• Participate in the assessment and forecasting of future trends and challenges in surgical robotics, adjusting strategies accordingly.

Team Management and Development

• Directly oversee and manage a multidisciplinary team, potentially including 1-5 members consisting of clinical engineers, medical science liaisons, and preclinical operations staff. Cultivate a culture of excellence, innovation, and continuous learning within the team.
• Provide mentorship and career development opportunities for team members.

Clinical Research and Innovation 

• Co-develop advanced clinical research initiatives in surgical robotics, ensuring they align with the latest medical standards and patient safety protocols. Participate in oversight of the entire lifecycle of clinical research projects, from conception through to publication.
• Drive innovation in surgical robotics, staying ahead of technological advancements and competitive developments.
• Act as a strategic partner with medical evidence generation colleagues in Preclinical Research, Clinical Development, and Health Economics Market Access teams to develop and execute global strategies for evidence generation for new and existing products to support regulatory approval/clearance, health technology assessment, customer access, and post-marketing support.
• Provide scientific and medical perspectives for management of requests for Educational Grants, requests for Scientific Information, and requests for Investigator Initiated Research Grants.
• Provide critical evaluation of current literature and competitive activity, and in other domains where medical and scientific expertise is required.

Regulatory Compliance and Ethical Standards

• Ensure strict adherence to all relevant regulatory and ethical standards, including FDA regulations and international compliance requirements. Partner with colleagues in Regulatory for the preparation and submission of regulatory documents and reports.
• Maintain the highest ethical standards in all research and development activities.

Stakeholder Engagement and Communication

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