Medical Director (m/f) Ethicon Surgical Care and Energy - EMEA-00000OUY
Beschreibung
Johnson & Johnson MEDICAL GmbH is a subsidiary of the Johnson & Johnson group acting worldwide with more than 129,000 employees. Since 1930, our responsibility towards our staff has been, and still is, an essential element of our Credo. High quality standards and an inspiring identification with our products and services distinguish us. Johnson & Johnson MEDICAL GmbH is a trendsetter in the area of medical technology.
The Medical Director Ethicon Surgical Care and Energy will have both a regional medical affairs responsibility in support of the Ethicon Surgical Care and Energy business of the Johnson & Johnson Global Surgery Group and a local responsibility for all GSG medical affairs in Germany.
The position will report directly to the EMEA Medical Affairs Group Director.
Regional function
- Leads and drives Ethicon Surgical Care and Energy Medical Affairs in order to achieve the strategic goals and activities of the function, which consist of external facing (driving deeper and broader customer engagement; WW customer insight generation) and internal facing (clinical strategy, pipeline engagement, medical support of marketed products, compliance)
- Oversees and provides support of the New Product Development and New Business Development teams by providing expert medical and scientific input, including conceptual and hands-on product evaluation, and clinical research perspectives
- Evaluate and transfer to the R&D department innovative ideas coming from the surgical field who are deemed worth further investigation
- Oversee and act as a strategic partner with medical evidence generation colleagues in Preclinical Research, Clinical Development, and Health Economics and Reimbursement teams to develop and execute global strategies for evidence generation for new and existing products in order to support regulatory approval/clearance, health technology assessment, customer access, and post-marketing support
- Partner with Clinical Development to oversee and provide scientific and medical expertise required for conception and high quality design, execution, analysis, and reporting of clinical research in assigned areas. Clinical research skills will be required both for primarily regulatory purposes and for publication, to achieve market access, and to inform optimal practice
- Oversee and provide expert medical support to Regulatory Affairs, Communications, Legal, and QA/Risk Management / Product Safety teams
- Oversee and provide scientific and medical accountability for management of requests for Educational Grants, requests for Scientific Information, and requests for Investigator Initiated Research Grants
- Oversee and provide support of commercial teams by providing medical and scientific expertise to drive optimal business strategic direction and tactical business activities, including product launches, key scientific meetings, relationship management with leading research physicians and medical delivery system or government decision makers, critical evaluation of current literature and competitive activity, and in other domains where medical and scientific expertise is required
- Provides expert support to the EMEA Chief Safety Officer for the MD&D sector
Local function
- As the unique Medical Affairs point of contact for GSG in Germany, will follow and make sure that all medical support requests are appropriately and timely answered through the global Medical Affairs organization
- Present and discuss scientific data related to GSG products to the German public health authorities or private organizations such as the main buying groups
- Provide medical support to the different BUs of the German Global Surgery Group with a particular attention to prioritizing the requests according to the business priorities
Qualifikationen
- The candidate must be a Medical Doctor with a certification in General Surgery or another surgical specialization. A solid experience in surgical practice is required
- A strong background and experience in clinical research (medical device, biologics, and/or drugs, or combination products) including design and analysis of clinical research is required
- Experience managing healthcare professionals and/or clinical research professionals is required
- Experience in Healthcare industry is highly preferred
- Experience in support of European regulatory submissions is highly preferred
- Demonstrated business acumen, leadership skills, mentoring skills and the ability to make quick decisions
- Excellent communication skills, including written communication (e.g., peer review publication) and oral presentation of scientific materials and research results. Ability to write original scientific documents such as clinical summaries, regulatory filings, investigator brochures, and internal reports and scientific publications
- Ability to communicate effectively, orally and in writing, with many levels of employees of various disciplines within various departments
- Ability to build successful relationships with key opinion leaders globally and investigators in key business areas
- Excellent people management, public speaking, communication, leadership, organizational, interpersonal, and reasoning skills
- Teaching skills, including both oral and hands-on education of health care professionals and company employees on scientific and medical issues surrounding company products and on optimal safe and effective use of products
- Experience in Medical Safety and Surveillance appreciated
- Up to 25% travel (domestic and international) is required
- Fluent English and German
The well-being and development of our employees are central aspects of our company creed. Individuals who would like to fully realize their potential as part of our international, innovation-driven corporate family and who aspire to have challenging work, will find that our company provides just the right conditions. We consider intensive initial training, further education that is tailored to our employees' work, and excellent opportunities for development – both nationally and internationally – to be just as essential as a good work-life balance, attractive compensation and above-average employee benefits. One aspect that distinguishes our company is the large number of measures we have to support our trainees and promote career development in ways that are also compatible with family life.
Primärer Standort: Europa/mittlerer Osten/Afrika-Deutschland
Organisation: Johnson&Johnson Med GmbH (7930)
Funktion: Medical Affairs
Beschreibung
Johnson & Johnson MEDICAL GmbH is a subsidiary of the Johnson & Johnson group acting worldwide with more than 129,000 employees. Since 1930, our responsibility towards our staff has been, and still is, an essential element of our Credo. High quality standards and an inspiring identification with our products and services distinguish us. Johnson & Johnson MEDICAL GmbH is a trendsetter in the area of medical technology.
The Medical Director Ethicon Surgical Care and Energy will have both a regional medical affairs responsibility in support of the Ethicon Surgical Care and Energy business of the Johnson & Johnson Global Surgery Group and a local responsibility for all GSG medical affairs in Germany.
The position will report directly to the EMEA Medical Affairs Group Director.
Regional function
- Leads and drives Ethicon Surgical Care and Energy Medical Affairs in order to achieve the strategic goals and activities of the function, which consist of external facing (driving deeper and broader customer engagement; WW customer insight generation) and internal facing (clinical strategy, pipeline engagement, medical support of marketed products, compliance)
- Oversees and provides support of the New Product Development and New Business Development teams by providing expert medical and scientific input, including conceptual and hands-on product evaluation, and clinical research perspectives
- Evaluate and transfer to the R&D department innovative ideas coming from the surgical field who are deemed worth further investigation
- Oversee and act as a strategic partner with medical evidence generation colleagues in Preclinical Research, Clinical Development, and Health Economics and Reimbursement teams to develop and execute global strategies for evidence generation for new and existing products in order to support regulatory approval/clearance, health technology assessment, customer access, and post-marketing support
- Partner with Clinical Development to oversee and provide scientific and medical expertise required for conception and high quality design, execution, analysis, and reporting of clinical research in assigned areas. Clinical research skills will be required both for primarily regulatory purposes and for publication, to achieve market access, and to inform optimal practice
- Oversee and provide expert medical support to Regulatory Affairs, Communications, Legal, and QA/Risk Management / Product Safety teams
- Oversee and provide scientific and medical accountability for management of requests for Educational Grants, requests for Scientific Information, and requests for Investigator Initiated Research Grants
- Oversee and provide support of commercial teams by providing medical and scientific expertise to drive optimal business strategic direction and tactical business activities, including product launches, key scientific meetings, relationship management with leading research physicians and medical delivery system or government decision makers, critical evaluation of current literature and competitive activity, and in other domains where medical and scientific expertise is required
- Provides expert support to the EMEA Chief Safety Officer for the MD&D sector
Local function
- As the unique Medical Affairs point of contact for GSG in Germany, will follow and make sure that all medical support requests are appropriately and timely answered through the global Medical Affairs organization
- Present and discuss scientific data related to GSG products to the German public health authorities or private organizations such as the main buying groups
- Provide medical support to the different BUs of the German Global Surgery Group with a particular attention to prioritizing the requests according to the business priorities
Qualifikationen
- The candidate must be a Medical Doctor with a certification in General Surgery or another surgical specialization. A solid experience in surgical practice is required
- A strong background and experience in clinical research (medical device, biologics, and/or drugs, or combination products) including design and analysis of clinical research is required
- Experience managing healthcare professionals and/or clinical research professionals is required
- Experience in Healthcare industry is highly preferred
- Experience in support of European regulatory submissions is highly preferred
- Demonstrated business acumen, leadership skills, mentoring skills and the ability to make quick decisions
- Excellent communication skills, including written communication (e.g., peer review publication) and oral presentation of scientific materials and research results. Ability to write original scientific documents such as clinical summaries, regulatory filings, investigator brochures, and internal reports and scientific publications
- Ability to communicate effectively, orally and in writing, with many levels of employees of various disciplines within various departments
- Ability to build successful relationships with key opinion leaders globally and investigators in key business areas
- Excellent people management, public speaking, communication, leadership, organizational, interpersonal, and reasoning skills
- Teaching skills, including both oral and hands-on education of health care professionals and company employees on scientific and medical issues surrounding company products and on optimal safe and effective use of products
- Experience in Medical Safety and Surveillance appreciated
- Up to 25% travel (domestic and international) is required
- Fluent English and German
The well-being and development of our employees are central aspects of our company creed. Individuals who would like to fully realize their potential as part of our international, innovation-driven corporate family and who aspire to have challenging work, will find that our company provides just the right conditions. We consider intensive initial training, further education that is tailored to our employees' work, and excellent opportunities for development – both nationally and internationally – to be just as essential as a good work-life balance, attractive compensation and above-average employee benefits. One aspect that distinguishes our company is the large number of measures we have to support our trainees and promote career development in ways that are also compatible with family life.
Primärer Standort: Europa/mittlerer Osten/Afrika-Deutschland
Organisation: Johnson&Johnson Med GmbH (7930)
Funktion: Medical Affairs