Large

Intuitive (Nasdaq: ISRG), headquartered in Sunnyvale, Calif., is a global technology leader in minimally invasive care and the pioneer of robotic-assisted surgery. At Intuitive, we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.

Intuitive

Manufacturing

A global technology leader in minimally invasive care and the
pioneer of robotic-assisted surgery.

Science & Healthcare

You need a relevant degree, 3+ years in clinical monitoring, project management skills, fluency in English (additional European language preferred), travel readiness, and strong IT and communication skills.

You will assist in study protocol development, monitor studies, conduct site visits, ensure compliance, manage documentation, and support team training and process improvements.

Research & Development

Healthcare

Freiburg im Breisgau

Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As pioneer and leading company in the field of robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare’s hardest challenges and advance what is possible. Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere—we strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves. Passionate people who want to make a difference drive our culture—our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real-world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential. Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let’s advance the world of minimally invasive care. Job Description Primary Function of Position: The Clinical Research Associate (CRA) is a critical role principally performing remote on-site or in-house monitoring of clinical research studies data within his/her assigned projects in the region covered by Clinical Affairs. The candidate will ensure clinical trial conduct in compliance with applicable laws regulations MDD/MDR, ISO14155, guidance Good Clinical Practices (GCP), and Intuitive Surgical SOPs. This position will report to Clinical Affairs Europe, Intuitive Surgical Headquarters, in Switzerland. Roles & Responsibilities * Assist Clinical Affairs Manager (CAM)/Clinical Affairs Project Manager (CAPM) in protocol development, CRF designs and study documentation preparation for both pre-market and post market clinical studies. * Monitoring responsibility for smaller studies. * Conduct of on-site initiation visits, routine monitoring visits and closeout visits for both pre- and post-CE Mark studies. * Remote clinical database monitoring and query follow up with the Investigational center(s) to address potential data discrepancies. * Maintain study documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation. * Evaluation of the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. * Trouble-shoot with alignment of the CAPM any compliance issues at sites. * Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment, and enrollment, CRF completion and data query generation and resolution. * Maintains site performance metrics and implements action plans for sites not meeting expectations. * Assist in preparation and submission of regulatory packages to ethics committees and/or competent authorities. * Support the CAM/CPAM in the management of the study such as development of monitoring tools, source document templates, CRF completion guidelines, Clinical Monitoring Plans. * Develop additional study tools specific to the project or sites needs as required. * Support EDC testing for newly implemented databases. * Introduce Clinical Research Associates new to the position or company. * Support process improvement within Clinical Affairs. Qualifications Required Knowledge, Skills, and Experience: * Bachelor’s degree in science/health care field or nursing degree. * Experience working in medical device industry in the Clinical Affairs/research function with evidence of full monitoring responsibilities for at least three years. Experience of monitoring responsibilities for pre-CE mark European clinical studies is preferred. * Ability to manage multiple projects and varied tasks to meet deadlines. * English language required and a second European language preferred (French or German). * Ability and willingness to travel up to 25% of the time which may include several European countries. * Advanced knowledge of clinical research activities essential for both pre-CE and post-CE mark clinical studies. * Knowledge of applicable regulations (MDR, GCP, ISO-14155, MEDDEV guidelines, GDPR and applicable local regulations). * Strong analytical and problem-solving skills, and flexibility to change. * Strong IT skills; including use of eCRF and CTMS for monitoring, analytics, and MS Office tools. * Excellent written, verbal communication, and presentation skills. Additional Information Intuitive ist ein Arbeitgeber, der gleiche und gerechte Beschäftigungsmöglichkeiten bietet. Wir bieten allen qualifizierten Bewerbern und Mitarbeitern gleiche Beschäftigungsmöglichkeiten, unabhängig von ethnischer Herkunft, Geschlecht, Schwangerschaft, sexueller Orientierung, Geschlechtsidentität, nationaler Herkunft, Hautfarbe, Alter, Religion, geschütztem Veteranenstatus, Behindertenstatus, genetischen Informationen oder einem anderen Status, der nach den geltenden Gesetzen auf Bundes-, Landes- oder lokaler Ebene geschützt ist, und verbieten jegliche Form von Diskriminierung und Belästigung. Gemäß den „Fair Chance“-Gesetzen berücksichtigen wir qualifizierte Bewerber, die verhaftet wurden oder Vorstrafen haben, für offene Stellen. Shift: Day Travel: 25% of the time

Company DescriptionAt Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.As pioneer and leading company in the field of robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare’s hardest challenges and advance what is possible.Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere—we strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves.Passionate people who want to make a difference drive our culture—our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real-world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential.Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let’s advance the world of minimally invasive care.Job DescriptionPrimary Function of Position:The Clinical Research Associate (CRA) is a critical role principally performing remote on-site or in-house monitoring of clinical research studies data within his/her assigned projects in the region covered by Clinical Affairs. The candidate will ensure clinical trial conduct in compliance with applicable laws regulations MDD/MDR, ISO14155, guidance Good Clinical Practices (GCP), and Intuitive Surgical SOPs. This position will report to Clinical Affairs Europe, Intuitive Surgical Headquarters, in Switzerland.Roles & Responsibilities * Assist Clinical Affairs Manager (CAM)/Clinical Affairs Project Manager (CAPM) in protocol development, CRF designs and study documentation preparation for both pre-market and post market clinical studies. * Monitoring responsibility for smaller studies. * Conduct of on-site initiation visits, routine monitoring visits and closeout visits for both pre- and post-CE Mark studies. * Remote clinical database monitoring and query follow up with the Investigational center(s) to address potential data discrepancies. * Maintain study documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation. * Evaluation of the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. * Trouble-shoot with alignment of the CAPM any compliance issues at sites. * Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment, and enrollment, CRF completion and data query generation and resolution. * Maintains site performance metrics and implements action plans for sites not meeting expectations. * Assist in preparation and submission of regulatory packages to ethics committees and/or competent authorities. * Support the CAM/CPAM in the management of the study such as development of monitoring tools, source document templates, CRF completion guidelines, Clinical Monitoring Plans. * Develop additional study tools specific to the project or sites needs as required. * Support EDC testing for newly implemented databases. * Introduce Clinical Research Associates new to the position or company. * Support process improvement within Clinical Affairs.      QualificationsRequired Knowledge, Skills, and Experience: * Bachelor’s degree in science/health care field or nursing degree. * Experience working in medical device industry in the Clinical Affairs/research function with evidence of full monitoring responsibilities for at least three years. Experience of monitoring responsibilities for pre-CE mark European clinical studies is preferred. * Ability to manage multiple projects and varied tasks to meet deadlines. * English language required and a second European language preferred (French or German). * Ability and willingness to travel up to 25% of the time which may include several European countries. * Advanced knowledge of clinical research activities essential for both pre-CE and post-CE mark clinical studies. * Knowledge of applicable regulations (MDR, GCP, ISO-14155, MEDDEV guidelines, GDPR and applicable local regulations). * Strong analytical and problem-solving skills, and flexibility to change. * Strong IT skills; including use of eCRF and CTMS for monitoring, analytics, and MS Office tools. * Excellent written, verbal communication, and presentation skills.      Additional InformationIntuitive ist ein Arbeitgeber, der gleiche und gerechte Beschäftigungsmöglichkeiten bietet. Wir bieten allen qualifizierten Bewerbern und Mitarbeitern gleiche Beschäftigungsmöglichkeiten, unabhängig von ethnischer Herkunft, Geschlecht, Schwangerschaft, sexueller Orientierung, Geschlechtsidentität, nationaler Herkunft, Hautfarbe, Alter, Religion, geschütztem Veteranenstatus, Behindertenstatus, genetischen Informationen oder einem anderen Status, der nach den geltenden Gesetzen auf Bundes-, Landes- oder lokaler Ebene geschützt ist, und verbieten jegliche Form von Diskriminierung und Belästigung.Gemäß den „Fair Chance“-Gesetzen berücksichtigen wir qualifizierte Bewerber, die verhaftet wurden oder Vorstrafen haben, für offene Stellen.Shift: DayTravel: 25% of the time

Clinical Research Associate - Intuitive

&lt;strong&gt;Company Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.&lt;br&gt;&lt;br&gt;As pioneer and leading company in the field of robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare’s hardest challenges and advance what is possible.&lt;br&gt;&lt;br&gt;Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere—we strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves.&lt;br&gt;&lt;br&gt;Passionate people who want to make a difference drive our culture—our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real-world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential.&lt;br&gt;&lt;br&gt;Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let’s advance the world of minimally invasive care.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Job Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Primary Function of Position:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;The Clinical Research Associate (CRA) is a critical role principally performing remote on-site or in-house monitoring of clinical research studies data within his/her assigned projects in the region covered by Clinical Affairs. The candidate will ensure clinical trial conduct in compliance with applicable laws regulations MDD/MDR, ISO14155, guidance Good Clinical Practices (GCP), and Intuitive Surgical SOPs. This position will report to Clinical Affairs Europe, Intuitive Surgical Headquarters, in Switzerland.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Roles &amp;amp; Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Assist Clinical Affairs Manager (CAM)/Clinical Affairs Project Manager (CAPM) in protocol development, CRF designs and study documentation preparation for both pre-market and post market clinical studies.&lt;/li&gt;&lt;li&gt;Monitoring responsibility for smaller studies.&lt;/li&gt;&lt;li&gt;Conduct of on-site initiation visits, routine monitoring visits and closeout visits for both pre- and post-CE Mark studies.&lt;/li&gt;&lt;li&gt;Remote clinical database monitoring and query follow up with the Investigational center(s) to address potential data discrepancies.&lt;/li&gt;&lt;li&gt;Maintain study documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation.&lt;/li&gt;&lt;li&gt;Evaluation of the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.&lt;/li&gt;&lt;li&gt;Trouble-shoot with alignment of the CAPM any compliance issues at sites.&lt;/li&gt;&lt;li&gt;Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment, and enrollment, CRF completion and data query generation and resolution.&lt;/li&gt;&lt;li&gt;Maintains site performance metrics and implements action plans for sites not meeting expectations.&lt;/li&gt;&lt;li&gt;Assist in preparation and submission of regulatory packages to ethics committees and/or competent authorities.&lt;/li&gt;&lt;li&gt;Support the CAM/CPAM in the management of the study such as development of monitoring tools, source document templates, CRF completion guidelines, Clinical Monitoring Plans.&lt;/li&gt;&lt;li&gt;Develop additional study tools specific to the project or sites needs as required.&lt;/li&gt;&lt;li&gt;Support EDC testing for newly implemented databases.&lt;/li&gt;&lt;li&gt;Introduce Clinical Research Associates new to the position or company.&lt;/li&gt;&lt;li&gt;Support process improvement within Clinical Affairs.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Required Knowledge, Skills, and Experience: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Bachelor’s degree in science/health care field or nursing degree.&lt;/li&gt;&lt;li&gt;Experience working in medical device industry in the Clinical Affairs/research function with evidence of full monitoring responsibilities for at least three years. Experience of monitoring responsibilities for pre-CE mark European clinical studies is preferred.&lt;/li&gt;&lt;li&gt;Ability to manage multiple projects and varied tasks to meet deadlines.&lt;/li&gt;&lt;li&gt;English language required and a second European language preferred (French or German).&lt;/li&gt;&lt;li&gt;Ability and willingness to travel up to 25% of the time which may include several European countries.&lt;/li&gt;&lt;li&gt;Advanced knowledge of clinical research activities essential for both pre-CE and post-CE mark clinical studies.&lt;/li&gt;&lt;li&gt;Knowledge of applicable regulations (MDR, GCP, ISO-14155, MEDDEV guidelines, GDPR and applicable local regulations).&lt;/li&gt;&lt;li&gt;Strong analytical and problem-solving skills, and flexibility to change.&lt;/li&gt;&lt;li&gt;Strong IT skills; including use of eCRF and CTMS for monitoring, analytics, and MS Office tools.&lt;/li&gt;&lt;li&gt;Excellent written, verbal communication, and presentation skills.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Additional Information&lt;br&gt;&lt;br&gt;Intuitive ist ein Arbeitgeber, der gleiche und gerechte Beschäftigungsmöglichkeiten bietet. Wir bieten allen qualifizierten Bewerbern und Mitarbeitern gleiche Beschäftigungsmöglichkeiten, unabhängig von ethnischer Herkunft, Geschlecht, Schwangerschaft, sexueller Orientierung, Geschlechtsidentität, nationaler Herkunft, Hautfarbe, Alter, Religion, geschütztem Veteranenstatus, Behindertenstatus, genetischen Informationen oder einem anderen Status, der nach den geltenden Gesetzen auf Bundes-, Landes- oder lokaler Ebene geschützt ist, und verbieten jegliche Form von Diskriminierung und Belästigung.&lt;br&gt;&lt;br&gt;Gemäß den „Fair Chance“-Gesetzen berücksichtigen wir qualifizierte Bewerber, die verhaftet wurden oder Vorstrafen haben, für offene Stellen.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Shift:&lt;/strong&gt; Day&lt;br&gt;&lt;br&gt;&lt;strong&gt;Travel:&lt;/strong&gt; 25% of the time

Clinical Research Associate

Switzerland

You should have training experience, clinical knowledge, strong problem-solving and communication skills, adaptability, and a commitment to self-development, preferably with medical-device expertise.

You will conduct training for surgeons and teams, support specialized programs, manage logistics, develop training materials, gather feedback, and maintain da Vinci® equipment. Travel required.

Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare’s hardest challenges and advance what is possible. Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere—we strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves. Passionate people who want to make a difference drive our culture—our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real-world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential. Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let’s advance the world of minimally invasive care. Job Description Primary Function of Position: The Customer Trainer will report directly to the Senior Manager or Training Manager for their region. This training professional will deliver da Vinci® System technology training and facilitate surgeon-led training for surgeons, first assistants, and OR staff from a variety of surgical specialties including urology, gynecology, general surgery thoracic and Trans-oral surgery. The Customer Trainer will be actively involved in the continuous improvement of training programs and provide support for customer training, engineering, and training research initiatives. Roles And Responsibilities * Conduct da Vinci® and Ion training programs for surgeons, physicians, and their care teams at designated training centers and remote centers. * Lead and support Specialized training programs and Society events * This includes supporting the needs of the surgeon educators and course participants Conduct surveys to gather data and measure program effectiveness. * Act as subject matter expert for internal projects, as needed. * New product development Training material/ protocol development * Training research initiatives Work with the Training team in a creative, dependable, and flexible manner to improve existing training programs. * Train the sales force to conduct in-services and system technology skills development activities with customers on new and established products. * Occasional support of the da Vinci® System in a hospital operating room * Support da Vinci® Surgical System troubleshooting and maintenance at the training center. * Manage training center logistics, inventory, and training calendars. * Maintain all capital equipment, including but not limited to the cleaning and sterilization of instruments and accessories. * Support positive relationships between external training center personnel and ISI management. * Contribute to the organization’s quarterly goal achievements. * Develop competency in the following: da Vinci® System and Ion Technology, da Vinci® System applications and advanced technology, OR Efficiency, Training Pathway process. * Act as a Medical Device Consultant (Medizinprodukteberater) in Austria and Germany, after appropriate training, as per legal requirement and provide guidance, insight, and support in the proper handling of Intuitive medical devices. * Maintaining competency and currency on technology training protocol following the onboarding program guidelines, and annual competency check * Training/coaching techniques/methodologies * Travel required. Qualifications Required Knowledge, Skills, and Experience: * Professional Training experience preferred. * Clinical and/or operating room experience preferred. * High capacity and excellent problem-solving skills. * Solid organizational skills and ability to operate independently. * Professional work ethic * Solution oriented * Excellent oral and written communication skills * Strong interpersonal skills * Knowledge of adult learning principles preferred. * High capacity to learn in a fast-paced environment. * Medical-device experience preferred. * Commitment to self-development * Ability to work in a team environment. * Ability to be flexible with hours of operation. Additional Information Intuitive ist ein Arbeitgeber, der gleiche und gerechte Beschäftigungsmöglichkeiten bietet. Wir bieten allen qualifizierten Bewerbern und Mitarbeitern gleiche Beschäftigungsmöglichkeiten, unabhängig von ethnischer Herkunft, Geschlecht, Schwangerschaft, sexueller Orientierung, Geschlechtsidentität, nationaler Herkunft, Hautfarbe, Alter, Religion, geschütztem Veteranenstatus, Behindertenstatus, genetischen Informationen oder einem anderen Status, der nach den geltenden Gesetzen auf Bundes-, Landes- oder lokaler Ebene geschützt ist, und verbieten jegliche Form von Diskriminierung und Belästigung. Gemäß den „Fair Chance“-Gesetzen berücksichtigen wir qualifizierte Bewerber, die verhaftet wurden oder Vorstrafen haben, für offene Stellen. Shift: Day Travel: 25% of the time

Company DescriptionAt Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare’s hardest challenges and advance what is possible.Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere—we strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves.Passionate people who want to make a difference drive our culture—our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real-world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential.Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let’s advance the world of minimally invasive care.Job DescriptionPrimary Function of Position:The Customer Trainer will report directly to the Senior Manager or Training Manager for their region. This training professional will deliver da Vinci® System technology training and facilitate surgeon-led training for surgeons, first assistants, and OR staff from a variety of surgical specialties including urology, gynecology, general surgery thoracic and Trans-oral surgery. The Customer Trainer will be actively involved in the continuous improvement of training programs and provide support for customer training, engineering, and training research initiatives.Roles And Responsibilities * Conduct da Vinci® and Ion training programs for surgeons, physicians, and their care teams at designated training centers and remote centers. * Lead and support Specialized training programs and Society events * This includes supporting the needs of the surgeon educators and course participants Conduct surveys to gather data and measure program effectiveness. * Act as subject matter expert for internal projects, as needed. * New product development Training material/ protocol development * Training research initiatives Work with the Training team in a creative, dependable, and flexible manner to improve existing training programs. * Train the sales force to conduct in-services and system technology skills development activities with customers on new and established products. * Occasional support of the da Vinci® System in a hospital operating room * Support da Vinci® Surgical System troubleshooting and maintenance at the training center. * Manage training center logistics, inventory, and training calendars. * Maintain all capital equipment, including but not limited to the cleaning and sterilization of instruments and accessories. * Support positive relationships between external training center personnel and ISI management. * Contribute to the organization’s quarterly goal achievements. * Develop competency in the following: da Vinci® System and Ion Technology, da Vinci® System applications and advanced technology, OR Efficiency, Training Pathway process. * Act as a Medical Device Consultant (Medizinprodukteberater) in Austria and Germany, after appropriate training, as per legal requirement and provide guidance, insight, and support in the proper handling of Intuitive medical devices. * Maintaining competency and currency on technology training protocol following the onboarding program guidelines, and annual competency check * Training/coaching techniques/methodologies * Travel required.      QualificationsRequired Knowledge, Skills, and Experience: * Professional Training experience preferred. * Clinical and/or operating room experience preferred. * High capacity and excellent problem-solving skills. * Solid organizational skills and ability to operate independently. * Professional work ethic * Solution oriented * Excellent oral and written communication skills * Strong interpersonal skills * Knowledge of adult learning principles preferred. * High capacity to learn in a fast-paced environment. * Medical-device experience preferred. * Commitment to self-development * Ability to work in a team environment. * Ability to be flexible with hours of operation.      Additional InformationIntuitive ist ein Arbeitgeber, der gleiche und gerechte Beschäftigungsmöglichkeiten bietet. Wir bieten allen qualifizierten Bewerbern und Mitarbeitern gleiche Beschäftigungsmöglichkeiten, unabhängig von ethnischer Herkunft, Geschlecht, Schwangerschaft, sexueller Orientierung, Geschlechtsidentität, nationaler Herkunft, Hautfarbe, Alter, Religion, geschütztem Veteranenstatus, Behindertenstatus, genetischen Informationen oder einem anderen Status, der nach den geltenden Gesetzen auf Bundes-, Landes- oder lokaler Ebene geschützt ist, und verbieten jegliche Form von Diskriminierung und Belästigung.Gemäß den „Fair Chance“-Gesetzen berücksichtigen wir qualifizierte Bewerber, die verhaftet wurden oder Vorstrafen haben, für offene Stellen.Shift: DayTravel: 25% of the time

Customer Trainer - Intuitive

&lt;strong&gt;Company Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.&lt;br&gt;&lt;br&gt;As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare’s hardest challenges and advance what is possible.&lt;br&gt;&lt;br&gt;Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere—we strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves.&lt;br&gt;&lt;br&gt;Passionate people who want to make a difference drive our culture—our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real-world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential.&lt;br&gt;&lt;br&gt;Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let’s advance the world of minimally invasive care.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Job Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Primary Function of Position:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;The Customer Trainer will report directly to the Senior Manager or Training Manager for their region. This training professional will deliver da Vinci® System technology training and facilitate surgeon-led training for surgeons, first assistants, and OR staff from a variety of surgical specialties including urology, gynecology, general surgery thoracic and Trans-oral surgery. The Customer Trainer will be actively involved in the continuous improvement of training programs and provide support for customer training, engineering, and training research initiatives.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Roles And Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Conduct da Vinci® and Ion training programs for surgeons, physicians, and their care teams at designated training centers and remote centers.&lt;/li&gt;&lt;li&gt;Lead and support Specialized training programs and Society events&lt;/li&gt;&lt;li&gt;This includes supporting the needs of the surgeon educators and course participants Conduct surveys to gather data and measure program effectiveness. &lt;/li&gt;&lt;li&gt;Act as subject matter expert for internal projects, as needed.&lt;/li&gt;&lt;li&gt;New product development Training material/ protocol development &lt;/li&gt;&lt;li&gt;Training research initiatives Work with the Training team in a creative, dependable, and flexible manner to improve existing training programs.&lt;/li&gt;&lt;li&gt;Train the sales force to conduct in-services and system technology skills development activities with customers on new and established products. &lt;/li&gt;&lt;li&gt;Occasional support of the da Vinci® System in a hospital operating room &lt;/li&gt;&lt;li&gt;Support da Vinci® Surgical System troubleshooting and maintenance at the training center.&lt;/li&gt;&lt;li&gt;Manage training center logistics, inventory, and training calendars.&lt;/li&gt;&lt;li&gt;Maintain all capital equipment, including but not limited to the cleaning and sterilization of instruments and accessories. &lt;/li&gt;&lt;li&gt;Support positive relationships between external training center personnel and ISI management. &lt;/li&gt;&lt;li&gt;Contribute to the organization’s quarterly goal achievements. &lt;/li&gt;&lt;li&gt;Develop competency in the following: da Vinci® System and Ion Technology, da Vinci® System applications and advanced technology, OR Efficiency, Training Pathway process.&lt;/li&gt;&lt;li&gt;Act as a Medical Device Consultant (Medizinprodukteberater) in Austria and Germany, after appropriate training, as per legal requirement and provide guidance, insight, and support in the proper handling of Intuitive medical devices.&lt;/li&gt;&lt;li&gt;Maintaining competency and currency on technology training protocol following the onboarding program guidelines, and annual competency check&lt;/li&gt;&lt;li&gt;Training/coaching techniques/methodologies&lt;/li&gt;&lt;li&gt;Travel required.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Required Knowledge, Skills, and Experience:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Professional Training experience preferred.&lt;/li&gt;&lt;li&gt;Clinical and/or operating room experience preferred.&lt;/li&gt;&lt;li&gt;High capacity and excellent problem-solving skills.&lt;/li&gt;&lt;li&gt;Solid organizational skills and ability to operate independently.&lt;/li&gt;&lt;li&gt;Professional work ethic&lt;/li&gt;&lt;li&gt;Solution oriented&lt;/li&gt;&lt;li&gt;Excellent oral and written communication skills&lt;/li&gt;&lt;li&gt;Strong interpersonal skills&lt;/li&gt;&lt;li&gt;Knowledge of adult learning principles preferred.&lt;/li&gt;&lt;li&gt;High capacity to learn in a fast-paced environment.&lt;/li&gt;&lt;li&gt;Medical-device experience preferred.&lt;/li&gt;&lt;li&gt;Commitment to self-development&lt;/li&gt;&lt;li&gt;Ability to work in a team environment.&lt;/li&gt;&lt;li&gt;Ability to be flexible with hours of operation.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Additional Information&lt;br&gt;&lt;br&gt;Intuitive ist ein Arbeitgeber, der gleiche und gerechte Beschäftigungsmöglichkeiten bietet. Wir bieten allen qualifizierten Bewerbern und Mitarbeitern gleiche Beschäftigungsmöglichkeiten, unabhängig von ethnischer Herkunft, Geschlecht, Schwangerschaft, sexueller Orientierung, Geschlechtsidentität, nationaler Herkunft, Hautfarbe, Alter, Religion, geschütztem Veteranenstatus, Behindertenstatus, genetischen Informationen oder einem anderen Status, der nach den geltenden Gesetzen auf Bundes-, Landes- oder lokaler Ebene geschützt ist, und verbieten jegliche Form von Diskriminierung und Belästigung.&lt;br&gt;&lt;br&gt;Gemäß den „Fair Chance“-Gesetzen berücksichtigen wir qualifizierte Bewerber, die verhaftet wurden oder Vorstrafen haben, für offene Stellen.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Shift:&lt;/strong&gt; Day&lt;br&gt;&lt;br&gt;&lt;strong&gt;Travel:&lt;/strong&gt; 25% of the time

Intuitive

Mission