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/.
For more than 130 years, diversity, equity inclusion (DEI) has been a part of our cultural fabric at Johnson Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.
We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson Johnson, we all belong.
Johnson Johnson MedTech Surgery is recruiting for a Associate Director Clinical and Preclinical, located in Santa Clara, California.
Johnson Johnson MedTech has been working to make surgery better for more than a century. With substantial breadth and depth in surgical technologies, orthopedic and interventional solutions, we aspire to improve and enhance medical care for people worldwide. Together, we are working to shape the future of health through differentiated products and services.
Johnson Johnson’s long-term vision is to use digital technology as part of a holistic approach to surgery across the episode of care to enhance surgical efficiency, promote better clinical outcomes and increase patient satisfaction. This unique position will provide clinical and preclinical scientific leadership for Johnson Johnson’s MONARCH Platform, collaborating closely with the multi-functional evidence teams including Medical, Clinical, Pre-clinical, and Health Economics and Market Access.
Responsibilities Include
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
· Lead team of clinical and preclinical research professionals to develop and deliver appropriate global evidence generation strategies (preclinical studies, postmarket studies, investigator initiated, real world evidence) aligned to RD, Regulatory, Professional Education and Commercial needs for the MONARCH Platform
· Ensure input and strong alignment from key regional MedTech leads and other strategically important countries/regions in the development of the clinical and preclinical evidence generation strategies
· Contribute and support the design of appropriate studies to meet premarket and postmarket needs
· Strengthen capability in and drive implementation of real-world evidence to deliver cost-effective evidence solutions
· Identify areas of highest impact for the MONARCH portfolio, create and implement solutions that significantly impact ROI, and communicate impact across the organization
· Develop network with key surgeons in the US and globally to assist in execution of the evidence strategy
· Lead teams to ensure appropriate interpretation and dissemination of all evidence generated, based on evidence dissemination strategy, including study reports, abstracts, manuscripts, etc.
· Support clinical and preclinical scientific discussions with regulatory agencies / notified bodies to drive support of the clinical, preclinical, and regulatory strategy, including proposed studies; review process of evidence generated for marketing authorization, line extensions, etc., including during sponsor regulatory inspections
· Provide scientific, technical, and strategic assessment and/or oversight on New Business Development opportunities, and support acquisition of innovative products/devices that will position our company for future growth and success
· Demonstrate the ability to influence, shape and lead teams
· Develop talent to provide strategic and scientific clinical and preclinical research capability, including responsibility for professional development of direct reports
· Have experience in effective management of project budget processes
· Through transparent leadership, be a key leader in developing a high-performing team with a global culture
· Build successful relationships internally and develop partnerships with key business partners and customers/investigators
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/.
For more than 130 years, diversity, equity inclusion (DEI) has been a part of our cultural fabric at Johnson Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.
We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson Johnson, we all belong.
Johnson Johnson MedTech Surgery is recruiting for a Associate Director Clinical and Preclinical, located in Santa Clara, California.
Johnson Johnson MedTech has been working to make surgery better for more than a century. With substantial breadth and depth in surgical technologies, orthopedic and interventional solutions, we aspire to improve and enhance medical care for people worldwide. Together, we are working to shape the future of health through differentiated products and services.
Johnson Johnson’s long-term vision is to use digital technology as part of a holistic approach to surgery across the episode of care to enhance surgical efficiency, promote better clinical outcomes and increase patient satisfaction. This unique position will provide clinical and preclinical scientific leadership for Johnson Johnson’s MONARCH Platform, collaborating closely with the multi-functional evidence teams including Medical, Clinical, Pre-clinical, and Health Economics and Market Access.
Responsibilities Include
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
· Lead team of clinical and preclinical research professionals to develop and deliver appropriate global evidence generation strategies (preclinical studies, postmarket studies, investigator initiated, real world evidence) aligned to RD, Regulatory, Professional Education and Commercial needs for the MONARCH Platform
· Ensure input and strong alignment from key regional MedTech leads and other strategically important countries/regions in the development of the clinical and preclinical evidence generation strategies
· Contribute and support the design of appropriate studies to meet premarket and postmarket needs
· Strengthen capability in and drive implementation of real-world evidence to deliver cost-effective evidence solutions
· Identify areas of highest impact for the MONARCH portfolio, create and implement solutions that significantly impact ROI, and communicate impact across the organization
· Develop network with key surgeons in the US and globally to assist in execution of the evidence strategy
· Lead teams to ensure appropriate interpretation and dissemination of all evidence generated, based on evidence dissemination strategy, including study reports, abstracts, manuscripts, etc.
· Support clinical and preclinical scientific discussions with regulatory agencies / notified bodies to drive support of the clinical, preclinical, and regulatory strategy, including proposed studies; review process of evidence generated for marketing authorization, line extensions, etc., including during sponsor regulatory inspections
· Provide scientific, technical, and strategic assessment and/or oversight on New Business Development opportunities, and support acquisition of innovative products/devices that will position our company for future growth and success
· Demonstrate the ability to influence, shape and lead teams
· Develop talent to provide strategic and scientific clinical and preclinical research capability, including responsibility for professional development of direct reports
· Have experience in effective management of project budget processes
· Through transparent leadership, be a key leader in developing a high-performing team with a global culture
· Build successful relationships internally and develop partnerships with key business partners and customers/investigators
· A minimum of a Bachelor’s degree in Biological Science or a related discipline is required. An advanced degree (Master’s or PhD) is preferred.
· A minimum of 8 years of related scientific / technical experience, including leadership / management role within Clinical and/or Preclinical Research is required.
· A minimum of 2 years of people management-related experience is required.
· Experience working in Robotics is strongly preferred.
· Expertise in clinical and preclinical science and processes along with a broad and extensive understanding of product development processes, team dynamics, related healthcare market environment, clinical trends, and global clinical trial regulations is required.
· Experience in support of global regulatory submissions for medical devices, biologics, or drugs (including PMA/BLA/NDA and/or their global counterparts) is preferred.
· Ability to lead a team of clinical and preclinical scientists to provide strategic and scientific research input across NPD and LCM projects is preferred.
· Proven track record of contributing to clinical and/or preclinical programs on time, within budget and in compliance to SOPs and regulations is required.
· This position will be located in Santa Clara, CA and may require up to 25% domestic and international travel.
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, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.
The anticipated base pay range for this position is 168,000 to 271000.
The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis.
Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).Employees are eligible for the following time off benefits: Vacation – up to 120 hours per calendar yearSick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar yearHoliday pay, including Floating Holidays – up to 13 days per calendar year of Work, Personal and Family Time - up to 40 hours per calendar yearAdditional information can be found through the link below. https://www.careers.jnj.com/employee-benefitsThe compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market."
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· A minimum of a Bachelor’s degree in Biological Science or a related discipline is required. An advanced degree (Master’s or PhD) is preferred.
· A minimum of 8 years of related scientific / technical experience, including leadership / management role within Clinical and/or Preclinical Research is required.
· A minimum of 2 years of people management-related experience is required.
· Experience working in Robotics is strongly preferred.
· Expertise in clinical and preclinical science and processes along with a broad and extensive understanding of product development processes, team dynamics, related healthcare market environment, clinical trends, and global clinical trial regulations is required.
· Experience in support of global regulatory submissions for medical devices, biologics, or drugs (including PMA/BLA/NDA and/or their global counterparts) is preferred.
· Ability to lead a team of clinical and preclinical scientists to provide strategic and scientific research input across NPD and LCM projects is preferred.
· Proven track record of contributing to clinical and/or preclinical programs on time, within budget and in compliance to SOPs and regulations is required.
· This position will be located in Santa Clara, CA and may require up to 25% domestic and international travel.
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, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.
The anticipated base pay range for this position is 168,000 to 271000.
The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis.
Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).Employees are eligible for the following time off benefits: Vacation – up to 120 hours per calendar yearSick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar yearHoliday pay, including Floating Holidays – up to 13 days per calendar year of Work, Personal and Family Time - up to 40 hours per calendar yearAdditional information can be found through the link below. https://www.careers.jnj.com/employee-benefitsThe compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market."
#LI-RP1