84 Jobs für Internal Medicine Expert
Stellenangebote Internal Medicine Expert Jobs
Job vor 2 Tagen bei StepStone gefunden
Fresenius Medical Care Deutschland GmbH
• Bad Homburg bei Frankfurt
[. .. ] the respective insurance lines and claims Administration of global Insurance programs, including policy issuance tracking and delivery, territorial analysis/ premium allocations remittances/ query resolution Provide global subject [...]
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[...] matter expertise to internal and external stakeholders Promote and drive compliance with the global end-to-end process with internal and external stakeholders Data input and coordination of global knowledge, workflow, network communication program administration tools First contact for insurance-related matters for the colleagues in foreign countries Preparation of reports, global policy summaries [. .. ] is a plus Fluent in English (written and spoken) German is required There is a lot you can discover at Fresenius Medical Care, regardless in which field you are an expert and how much experience you have all dedicated to your professional journey. Whether in front of or behind the scenes, you are helping to make ever-better medicine available to more and more people around the world Individual opportunities for self-determined career planning and professional development A corporate culture in which there is enough room for innovative thinking to find the best solution together, not the quickest one A large number of committed people with a wide [. .. ]
Job vor 14 Tagen bei Jobware gefunden
Deutsches Krebsforschungszentrum (DKFZ)
Scientific Coordinator
• Heidelberg
Jobticket
[. .. ] number: 2026-0040Heidelberg Full-time Intelligent Medical Systems The Division of Intelligent Medical Systems (IMSY) is an interdisciplinary research division working at the interface of computer science, physics, statistics, [...]
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[...] and medicine. Our mission is to address the unique methodological and translational challenges of medical imaging AI to enable robust, clinically meaningful applications, with a particular focus on surgical AI. IMSY is highly international and strongly embedded in large collaborative research consortia, meta-research initiatives, and community-driven projects. Project Description Artificial [. .. ] based on high-impact clinical questions. Through a large-scale global crowdsourcing campaign, experts worldwide are invited to submit clinically meaningful challenges together with corresponding imaging data. An international, multidisciplinary expert panel will identify those tasks whose solution would have clear relevance for patient care. MEDAL s objective is to create a rigorous and internationally recognized final exam for medical AI-a benchmark designed to assess whether advanced AI models can address complex clinical scenarios and demonstrate tangible clinical value, thereby [. .. ] and committee meetings, as well as their preparation and follow-up Central point of contact for national and international consortium partners Assistance with correspondence and communication Planning and organizing scientific conferences, internal events, Delphi rounds, crowdsourcing activities, workshops, and seminars Monitoring timelines, milestones, and deliverables across work packages Supporting concept development, grant writing, and report preparation Conducting surveys and translating findings into actionable items Planning and supporting workflow optimization and change processes in close collaboration with partners Overseeing budget and personnel to [. .. ]
Job vor 14 Tagen bei JobMESH gefunden
Deutsches Krebsforschungszentrum (DKFZ)
• Baden- Wurttemberg Heidelberg
Jobticket
[. .. ] number: 2026-0040Heidelberg Full-time Intelligent Medical Systems The Division of Intelligent Medical Systems (IMSY) is an interdisciplinary research division working at the interface of computer science, physics, statistics, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and medicine. Our mission is to address the unique methodological and translational challenges of medical imaging AI to enable robust, clinically meaningful applications, with a particular focus on surgical AI. IMSY is highly international and strongly embedded in large collaborative research consortia, meta-research initiatives, and community-driven projects. Project Description Artificial [. .. ] based on high-impact clinical questions. Through a large-scale global crowdsourcing campaign, experts worldwide are invited to submit clinically meaningful challenges together with corresponding imaging data. An international, multidisciplinary expert panel will identify those tasks whose solution would have clear relevance for patient care. MEDALs objective is to create a rigorous and internationally recognized final exam for medical AI-a benchmark designed to assess whether advanced AI models can address complex clinical scenarios and demonstrate tangible clinical value, thereby channeling [. .. ] and committee meetings, as well as their preparation and follow-up Central point of contact for national and international consortium partners Assistance with correspondence and communication Planning and organizing scientific conferences, internal events, Delphi rounds, crowdsourcing activities, workshops, and seminars Monitoring timelines, milestones, and deliverables across work packages Supporting concept development, grant writing, and report preparation Conducting surveys and translating findings into actionable items Planning and supporting workflow optimization and change processes in close collaboration with partners Overseeing budget and personnel to [. .. ]
Job am 11.03.2026 bei JobMESH gefunden
PAUL HARTMANN AG
Regulatory Affairs Expert-Manage Quality Regulatory Affairs-Pharmaceutical Industry (f/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] that make a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join [...]
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[...] our team as Expert Component Qualification (Qm/RA) (f/m/d) DEU-Heidenheim As Expert Component Qualification (Qm/RA) (f/m/d) for Procedure Packs, you will play a crucial role in ensuring our products meet regulatory and quality standards across global markets. You will serve as a key interface between development, marketing and [. .. ] offers you the opportunity to make a tangible impact on patient safety and innovation. Responsibilities: Manage Quality and Regulatory Affairs topics related to components for procedure packs in compliance with internal policies and external regulations Support development and marketing teams regarding component qualification Qualify suppliers and maintain up-to-date component documentation Develop, maintain, and deliver training for internal processes and work instructions Support internal and external audits, CAPAs, vigilance, and recall activities Conducting internal trainings on component qualification issues Qualifications: Completed degree in natural sciences, medicine, or a comparable technical discipline; alternatively, a technical qualification with relevant professional experience Formal training or hands-on experience in Regulatory Affairs is beneficial Solid understanding of Quality and Regulatory Affairs in the medical device or pharmaceutical industry Strong intercultural communication skills Analytical mindset with excellent problem-solving capabilities Proficient [. .. ]
Job am 11.03.2026 bei JobMESH gefunden
PAUL HARTMANN AG
• Baden- Wurttemberg Heidenheim
[. .. ] that make a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our team as Expert Component Qualification (Qm/RA) (f/m/d) DEU-Heidenheim As Expert Component Qualification (Qm/RA) (f/m/d) for Procedure Packs, you will play a crucial role in ensuring our products meet regulatory and quality standards across global markets. You will serve as a key interface between development, marketing and [. .. ] offers you the opportunity to make a tangible impact on patient safety and innovation. Responsibilities: Manage Quality and Regulatory Affairs topics related to components for procedure packs in compliance with internal policies and external regulations Support development and marketing teams regarding component qualification Qualify suppliers and maintain up-to-date component documentation Develop, maintain, and deliver training for internal processes and work instructions Support internal and external audits, CAPAs, vigilance, and recall activities Conducting internal trainings on component qualification issues Qualifications: Completed degree in natural sciences, medicine, or a comparable technical discipline; alternatively, a technical qualification with relevant professional experience Formal training or hands-on experience in Regulatory Affairs is beneficial Solid understanding of Quality and Regulatory Affairs in the medical device or pharmaceutical industry Strong intercultural communication skills Analytical mindset with excellent problem-solving capabilities Proficient [. .. ]
Job am 11.03.2026 bei JobMESH gefunden
PAUL HARTMANN AG
Natural Scientist as Expert Component Qualification-Regulatory Affairs Topics (f/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] that make a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our team as Expert Component Qualification (Qm/RA) (f/m/d) DEU-Heidenheim As Expert Component Qualification (Qm/RA) (f/m/d) for Procedure Packs, you will play a crucial role in ensuring our products meet regulatory and quality standards across global markets. You will serve as a key interface between development, marketing and [. .. ] offers you the opportunity to make a tangible impact on patient safety and innovation. Responsibilities: Manage Quality and Regulatory Affairs topics related to components for procedure packs in compliance with internal policies and external regulations Support development and marketing teams regarding component qualification Qualify suppliers and maintain up-to-date component documentation Develop, maintain, and deliver training for internal processes and work instructions Support internal and external audits, CAPAs, vigilance, and recall activities Conducting internal trainings on component qualification issues Qualifications: Completed degree in natural sciences, medicine, or a comparable technical discipline; alternatively, a technical qualification with relevant professional experience Formal training or hands-on experience in Regulatory Affairs is beneficial Solid understanding of Quality and Regulatory Affairs in the medical device or pharmaceutical industry Strong intercultural communication skills Analytical mindset with excellent problem-solving capabilities Proficient [. .. ]
Job am 11.03.2026 bei JobMESH gefunden
PAUL HARTMANN AG
• Baden- Wurttemberg Heidenheim
[. .. ] that make a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our team as Expert Component Qualification (Qm/RA) (f/m/d) DEU-Heidenheim As Expert Component Qualification (Qm/RA) (f/m/d) for Procedure Packs, you will play a crucial role in ensuring our products meet regulatory and quality standards across global markets. You will serve as a key interface between development, marketing and [. .. ] offers you the opportunity to make a tangible impact on patient safety and innovation. Responsibilities: Manage Quality and Regulatory Affairs topics related to components for procedure packs in compliance with internal policies and external regulations Support development and marketing teams regarding component qualification Qualify suppliers and maintain up-to-date component documentation Develop, maintain, and deliver training for internal processes and work instructions Support internal and external audits, CAPAs, vigilance, and recall activities Conducting internal trainings on component qualification issues Qualifications: Completed degree in natural sciences, medicine, or a comparable technical discipline; alternatively, a technical qualification with relevant professional experience Formal training or hands-on experience in Regulatory Affairs is beneficial Solid understanding of Quality and Regulatory Affairs in the medical device or pharmaceutical industry Strong intercultural communication skills Analytical mindset with excellent problem-solving capabilities Proficient [. .. ]
Job am 03.03.2026 bei JobMESH gefunden
PAUL HARTMANN AG
Expert Component Qualification (Qm/RA) (f/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] that make a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our team as Expert Component Qualification (Qm/RA) (f/m/d) DEU-Heidenheim As Expert Component Qualification (Qm/RA) (f/m/d) for Procedure Packs, you will play a crucial role in ensuring our products meet regulatory and quality standards across global markets. You will serve as a key interface between development, marketing and [. .. ] offers you the opportunity to make a tangible impact on patient safety and innovation. Responsibilities: Manage Quality and Regulatory Affairs topics related to components for procedure packs in compliance with internal policies and external regulations Support development and marketing teams regarding component qualification Qualify suppliers and maintain up-to-date component documentation Develop, maintain, and deliver training for internal processes and work instructions Support internal and external audits, CAPAs, vigilance, and recall activities Conducting internal trainings on component qualification issues Qualifications: Completed degree in natural sciences, medicine, or a comparable technical discipline; alternatively, a technical qualification with relevant professional experience Formal training or hands-on experience in Regulatory Affairs is beneficial Solid understanding of Quality and Regulatory Affairs in the medical device or pharmaceutical industry Strong intercultural communication skills Analytical mindset with excellent problem-solving capabilities Proficient [. .. ]
Job vor 7 Tagen bei Neuvoo.com gefunden
PAUL HARTMANN AG
Regulatory Affairs/ Quality Assurance Manager-Support Development Marketing (f/m/d)
• Baden- Württemberg
[. .. ] that make a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our team as Expert Component Qualification (Qm/RA) (f/m/d) DEU-Heidenheim As Expert Component Qualification (Qm/RA) (f/m/d) for Procedure Packs, you will play a crucial role in ensuring our products meet regulatory and quality standards across global markets. You will serve as a key interface between development, marketing and [. .. ] offers you the opportunity to make a tangible impact on patient safety and innovation. Responsibilities: Manage Quality and Regulatory Affairs topics related to components for procedure packs in compliance with internal policies and external regulations Support development and marketing teams regarding component qualification Qualify suppliers and maintain up-to-date component documentation Develop, maintain, and deliver training for internal processes and work instructions Support internal and external audits, CAPAs, vigilance, and recall activities Conducting internal trainings on component qualification issues Qualifications: Completed degree in natural sciences, medicine, or a comparable technical discipline; alternatively, a technical qualification with relevant professional experience Formal training or hands-on experience in Regulatory Affairs is beneficial Solid understanding of Quality and Regulatory Affairs in the medical device or pharmaceutical industry Strong intercultural communication skills Analytical mindset with excellent problem-solving capabilities Proficient [. .. ]
Job vor 14 Tagen bei JobMESH gefunden
PAUL HARTMANN AG
Regulatory Affairs Expert-Manage Quality Regulatory Affairs-Pharmaceutical Industry (f/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] that make a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our team as Expert Component Qualification (Qm/RA) (f/m/d) DEU-Heidenheim As Expert Component Qualification (Qm/RA) (f/m/d) for Procedure Packs, you will play a crucial role in ensuring our products meet regulatory and quality standards across global markets. You will serve as a key interface between development, marketing and [. .. ] offers you the opportunity to make a tangible impact on patient safety and innovation. Responsibilities: Manage Quality and Regulatory Affairs topics related to components for procedure packs in compliance with internal policies and external regulations Support development and marketing teams regarding component qualification Qualify suppliers and maintain up-to-date component documentation Develop, maintain, and deliver training for internal processes and work instructions Support internal and external audits, CAPAs, vigilance, and recall activities Conducting internal trainings on component qualification issues Qualifications: Completed degree in natural sciences, medicine, or a comparable technical discipline; alternatively, a technical qualification with relevant professional experience Formal training or hands-on experience in Regulatory Affairs is beneficial Solid understanding of Quality and Regulatory Affairs in the medical device or pharmaceutical industry Strong intercultural communication skills Analytical mindset with excellent problem-solving capabilities Proficient [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
United Nations
• AT- 9 Wien
[. .. ] world-wide concerns of radiation hazards, such as fallout from nuclear weapons tests, assessments of nuclear accidents (e. g. , those at Chernobyl and Fukushima) , trends in [...]
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[...] exposure in medicine, and effects and risks to health from radiation exposures (e. g. , to radon) . (2) Coordinate the preparation of the annual UNSCEAR Reports submitted to the General Assembly and prepare scientifically robust technical documents which serve as basis for the substantive scientific annexes of the UNSCEAR Reports to the [. .. ] special aspects of levels and effects of radiation exposure to assess the attendant effects and risks for health and the environment. In consultation with the Committees Bureau: Select and engage expert scientists. Supervise and coordinate their work in preparing background and technical documents for review by the Committee. Substantiate the technical standards for conducting UNSCEAR evaluations, and the scientific consistency and validity of documents written at the request of the Committee by the Secretary, secretariat staff, consultants or experts to ensure [. .. ] funding source of the position, the eligibility for this temporary job opening may be limited to candidates based at the duty station. This temporary job opening may be limited to internal candidates, who have been recruited through a competitive examination administered according to staff rule 4.16 or staff selection process including the review of a central review body established according to staff rule 4.15. Staff members of the United Nations common system organizations who will reach the mandatory age [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
ITH Icoserve
CEECA Radiology Solutions Partner (m/f/d) X ray, Fluoro Mammography
• AT- 9 Wien
[. .. ] interesting? CEECA Radiology Solutions Partner (m/f/d) X ray, Fluoro Mammography Location: CEECA Zone (Remote) We are looking for someone with deep radiology expertise who enjoys acting as [...]
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[...] an internal advisor collaborating, guiding, and influencing through knowledge, competence, and professional credibility. This is an excellent opportunity to shape the radiology market with a strong focus on Womens Health across more than 30 countries in the CEECA zone. Your Tasks and Responsibilities Provide expert consultation to internal teams on X ray, fluoroscopy, and mammography systems. Advise on equipment selection, system specifications, and clinical workflows. Collaborate closely with internal stakeholders: Country Business Managers, Business Partners, and Sales. Support tender processes by preparing technical documentation and specifications. Deliver product presentations, demonstrations, and specialized workshops for internal [. .. ] healthcare. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. Our Culture Our culture embraces different perspectives, open debate, and the will to challenge convention. Change is a constant aspect of our work. We aspire to lead the change in our industry rather than just react to it. Thats why we invite [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
NEVEON Executive Committee
• KI Kremsmünster
Overview We are not offering you a job, but rather we are offering you a workplace that feels like home at Greiner Bio-One. Senior
Expert Medical and Scientific Affairs [...]
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[...] (all genders) Location: Kremsmünster, AT, 4550 Employment Type: Permanent Responsibilities Support our colleagues with your clinical and scientific expertise and experience in clinical diagnostics, contributing to the clinical and scientific knowledge base for Greiner Bio-One products Support the Clinical Studies team with regard to study [. .. ] marketing and educational purposes Coordinate and respond to customer inquiries Collaborate with the R D team, Product Managers and Product Application Specialists Your Profile You have completed your studies in Medicine, Biomedical Analytics, Biochemistry, Pharmacy or a similar discipline. An advanced degree (Ph D) is a plus but not required. You have gained experience as a Specialist in Clinical Chemistry and Laboratory Medicine, ideally with experience and a publication track record in preanalytical research phase. You have significant experience in a clinical [. .. ] have excellent English skills (Level C1 preferred) as well as a very good working knowledge of MS Office. You enjoy finding new approaches and solutions as well as communicating with internal and external partners. Membership of international professional organizations such as IFCC and EFLM is preferred. Our Offer A collaborative environment where diverse voices are valued and respected. Opportunities for professional growth and development. Flexibility in how you approach your work and balance your responsibilities. A culture that supports curiosity, continuous [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
Pfizer
Medical Review Manager (m/f/d)
• AT- 9 Wien
Homeoffice möglich
[. .. ] to continuous improvement by applying best practices, identifying new ways of working, and enhancing the value delivered to medical colleagues in-country. Role Responsibilities: Strategic Oversight Serve as [...]
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[...] Subject Matter Expert and main contact for Medical Review to enable fast, highquality deliverables. Identify strategic opportunities to improve incountry services, operations, and crossfunctional alignment. Analyze incountry metrics and provide strategic recommendations to leadership. Collaborate closely with CMAO categories and country teams to drive engagement with Medical and Marketing. Lead process documentation and continuous improvement initiatives. Provision of Medical Expertise Maintain strong scientific and clinical knowledge of Pfizer medicines and competitors. Advocate for appropriate medicine use within the local healthcare system. Collaboration to Enable Streamlined Content Creation Partner with crossfunctional teams to develop compliant and impactful promotional and nonpromotional materials. Provide medical, scientific, and regulatory guidance during content development. Review and advise on materials for health authority submissions, risk management plans, and a RMM. Support creation and review of internal training materials. Ensure all activities meet ethical standards and regulatory/ compliance requirements. Support needs of Medical, Marketing, corporate, and social media content. Engagement Cross Functional Support Build strong relationships with leadership and stakeholders to support continuous improvement. Coordinate incountry communication across functions and workflows. Support abovecountry activities compliant with local [. .. ]
Job am 08.03.2026 bei Mindmatch.ai gefunden
AOP Health
• AT- 9 Wien
Homeoffice möglich
[. .. ] trends and generate insights for Global and Affiliate stakeholders. Serve as the global escalation point for complex inquiries in collaboration with vendors and Global Medical Affairs. Act [...]
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[...] as subject matter expert for compliance topics including Pharmacovigilance, Regulatory Affairs, and Data Privacy. Support and optimize digital MI solutions (e. g. , Veeva Med Inquiry) and ensure data governance standards. Deliver product, system, and process trainings to internal teams and external partners. Ensure inspection readiness and adherence to SOPs, industry codes, and internal compliance standards. Collaborate crossfunctionally with Regulatory, PV, Legal, and Medical Affairs teams globally. Your Qualifications And Experience Advanced degree in Life Sciences, Pharmacy, or Medicine 5+ years of experience in Medical Information, Medical Affairs, or a related function within the pharmaceutical industry. Strong scientific background with excellent analytical and medical writing skills. Experience working with global teams and external vendors. Familiarity with Veeva Medical Information systems (e. g. , Med Inquiry) is an advantage. Solid [. .. ]
Job am 08.03.2026 bei Mindmatch.ai gefunden
OSCE
Chief Medical Officer (S)
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] Viennabased staff during office hours. Confirming the medical condition of dependents for the purpose of administering disabilityrelated benefits and entitlements to eligible OSCE officials; Sick leave and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] health monitoring: Providing expert advice and input on the development and revision of sick leave and healthrelated organizational policies and procedures. Carrying out returntowork evaluations in line with OSCE Staff Regulations and Staff Rules and other applicable administrative issuances; monitoring longterm sick leave cases, providing advice in sensitive or complex individual cases, and reviewing [. .. ] planning for adequate resourcing of OSC Ewide Occupational Safety and Health initiatives, including through development of strategic projects and resource mobilization efforts to advance occupational health priorities, maximizing external and internal funding opportunities; Coordination of medical services across the OSCE: Exercising functional authority over medical personnel across the Secretariat, Institutions and Field Operations to ensure compliance with established standards and professional practice. Establishing quality assurance mechanisms by facilitating policy and procedure harmonization and compliance among OSCE medical personnel; organizing professional development [. .. ] medical infrastructure in OSCE duty stations, including identification and evaluation of hospitals, clinics, pharmacies and emergency facilities to ensure adequate treatment and evacuation readiness. Necessary Qualifications A university degree in Medicine (MD) and licence to practice; specialization in occupational medicine, emergency medicine or healthcare management is highly desirable; Minimum of ten years of progressively responsible medical experience, preferably including international occupational health settings; Experience in development of health policies or procedures, strategic planning or emergency medical coordination; Strong analytical, interpersonal and [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Grünenthal Group
• AT- 9 Wien
[. .. ] youll take on diverse and stimulating challenges, such as: Leading the development, review, and execution of medical projects that advance the strategic objectives of the portfolio. Acting [...]
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[...] as the scientific expert for your therapeutic area, ensuring highquality medical information and strategic alignment across all initiatives. Supporting the Medical Information team through the development and review of Standard Response Documents, ensuring consistency, scientific rigor, and alignment with internal guidance. Acting as a delegate on behalf of the Informationsbeauftragter for DACH, ensuring compliance with regional regulatory and communication requirements. Serving as a strategic partner within brand teams, ensuring medical excellence in omnichannel engagement. Gathering and analyzing scientific insights from the field to inform medical and commercial strategies. Shaping the [. .. ] pharmacovigilance teams with your therapeutic expertise. What Youll Bring To The Table To make the most of this role and grow successfully, you should bring: A successfully completed degree in Medicine, Pharmacy, or a natural science discipline, ideally complemented by a Ph D. At least 3 years of relevant experience in the pharmaceutical industry. A deep understanding of the pharmaceutical environment and solid knowledge of the DACH healthcare systems. Comprehensive knowledge of applicable legal and regulatory requirements, with the ability to apply [. .. ]
Job gestern bei Jobleads gefunden
Chief Commercial and Engagement Officer
Führungs-/ Leitungspositionen
[. .. ] animal welfare landscape, celebrated for our compassionate care of around 18, 000 lost and abandoned dogs and cats every year. Beyond caring for animals, we provide diverse [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] services including veterinary medicine, behaviour, advocacy and community education programs, all aimed at giving animals the best chance of a happy and healthy life. Our mission is upheld by passionate individuals who embody a profound affinity for animals, community and advocacy. About the Role As a key member of the Executive Team, this role [. .. ] tertiary qualifications in Public Relations, Media, Marketing, Communications, Business, or equivalent experience. A strong track record of developing and scaling commercial initiatives that generate sustainable revenue and measurable community impact. Expert communications and media skills, including preparing speeches, press releases, and stakeholder communications for internal and external audiences, and representing the organisation publicly. Demonstrated success in delivering brand and marketing activities, and previous experience delivering advocacy strategies and approaches. Exceptional leadership skills, with experience leading multidisciplinary teams, driving change, and building organisational capability. Strong project management, analytical, and problemsolving skills, and an ability to prioritise [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
P S L Group is a global organisation dedicated to putting information at the service of
medicine. The companies and people of the P S L Group aim to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] improve medical care by serving those who need it, those who provide it and those who seek to improve it. Our primary purpose is to help clients increase the effectiveness of activities pertaining to scientific communication, medical education [. .. ] medical education. We publish medical education across a wide swath of medical specialties, including: Cardiology General and Family Practice Hematology Oncology Ophthalmology Urology Objective The Medical Director will collaborate with internal and external experts to complete the following key tasks: Identify existing practice gaps and underlying unmet needs (15) Develop strategic needs assessments/ proposals that align these practice gaps and unmet needs with innovative solutions to address these needs (20) Create high-quality content for medical education activities that meet established [. .. ] Solid editorial (writing and editing) skills and capability to adapt editorial style based on the educational format and/or the target audience (physicians, nurses, pharmacists, and other healthcare professionals) . Expert at Microsoft Office, specifically Power Point and Word. Comfortable working in a fast-paced, constantly evolving work environment. Proven ability to effectively set priorities, manage multiple projects/ assignments in various stages of development, and meet timelines, all while maintaining high quality standards. Positive, upbeat personality who communicates concisely and clearly, [. .. ]
Job am 08.03.2026 bei Jobleads gefunden
Chief Medical Officer (S)
• Wien
Führungs-/ Leitungspositionen
[. .. ] Viennabased staff during office hours. Confirming the medical condition of dependents for the purpose of administering disabilityrelated benefits and entitlements to eligible OSCE officials; Sick leave and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] health monitoring: Providing expert advice and input on the development and revision of sick leave and healthrelated organizational policies and procedures. Carrying out returntowork evaluations in line with OSCE Staff Regulations and Staff Rules and other applicable administrative issuances; monitoring longterm sick leave cases, providing advice in sensitive or complex individual cases, and reviewing [. .. ] planning for adequate resourcing of OSC Ewide Occupational Safety and Health initiatives, including through development of strategic projects and resource mobilization efforts to advance occupational health priorities, maximizing external and internal funding opportunities; Coordination of medical services across the OSCE: Exercising functional authority over medical personnel across the Secretariat, Institutions and Field Operations to ensure compliance with established standards and professional practice. Establishing quality assurance mechanisms by facilitating policy and procedure harmonization and compliance among OSCE medical personnel; organizing professional development [. .. ] medical infrastructure in OSCE duty stations, including identification and evaluation of hospitals, clinics, pharmacies and emergency facilities to ensure adequate treatment and evacuation readiness. Necessary Qualifications A university degree in Medicine (MD) and licence to practice; specialization in occupational medicine, emergency medicine or healthcare management is highly desirable; Minimum of ten years of progressively responsible medical experience, preferably including international occupational health settings; Experience in development of health policies or procedures, strategic planning or emergency medical coordination; Strong analytical, interpersonal and [. .. ]
Job am 01.03.2026 bei Jobleads gefunden
Medical Director Safety
• Lausanne, Waadt
Führungs-/ Leitungspositionen
[. .. ] develop and grow. Dont hesitate to connect with us during the recruitment process to learn more Position Summary As a Medical Director for Clinical Trial/ Research Safety [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you will provide expert safety leadership and input to clinical development programs for nutritional solutions and therapeutics across the lifespan, and ensure safety compliance with regulatory frameworks applicable to pharma, medical nutrition and food for medical purposes (FSMP) . A Day in the Life of a Medical Director Safety Responsible for building safety assessments [. .. ] Monitoring Boards charters, aggregate safety reports (DSUR/ ASR where applicable) , and risk management plans; contribute to Safety Risk Management Team (SRMT) and signal review forums Coordinate the management of internal trial safety boards and committees Drive safety strategies and ensure safety compliance with applicable regulatory frameworks, in close collaboration with clinical development, data management, medical, scientific and regulatory affairs teams as well as trusted external providers for case processing Engage with key opinion leaders (KOLs) and investigators, to shape safety [. .. ] dotted line alignment to internal patient safety risk management governance frameworks What Will Make You Successful Medical degree, Md/Ph D, preferably with specialization in one of the following areas: internal medicine/ gastroenterology/ pediatrics/ clinical pharmacology. Swiss medical practice license is a plus At least 5 years experience in clinical research and safety, in development or operations (pharma, biotech, diagnostics, medtech, nutrition, or CRO settings) Experience and proven impact in leading safety management in complex clinical trials, including issue management and regulatory [. .. ]
Job am 14.02.2026 bei Jobleads gefunden
Senior Director Medical Affairs-Neurology
• Ulm, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] Are Teva Were Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether its innovating in the fields of neuroscience and immunology or delivering [...]
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[...] high-quality medicine worldwide, were dedicated to addressing patients needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. Youll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. [. .. ] clinical, patient care, experience in Neurology. Five years pharmaceutical industry experience. Pharmaceutical industry experience in neurology. Experience in successfully developing strategy and executing medical plans, and in building professional external expert networks. Broad and good knowledge of drug development, clinical trial design, regulatory requirements, business development and life cycle management etc. SKILLS/ QUALIFICATIONS: Able to work in a changing and flexible environment with a strong patient focus and enterprise mindset. Experienced and adept at working collaboratively across different cross-functional teams [. .. ] pension scheme) . Function Medical Affairs Reports To Neuroscience lead, GMA Contact Sonia Buxeda Human Resources Already Working TEVA? If you are a current Teva employee, please apply using the internal career site available on Employee Central. By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site Tevas Equal Employment Opportunity Commitment Teva Pharmaceuticals is [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Medical Science Liaison (MSL) Gastroenterology (with fluent written and spoken German)
• Zug
[. .. ] healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, andsolutions are personal. Through our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise in Innovative Medicine and Med Tech, 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 jnj. com. As guided by Our Credo, Johnson Johnson is responsible to our employees who work with us [. .. ] their merit. Job Title Medical Science Liaison (MSL) Gastroenterology (with fluent written and spoken German) Department Medical Affairs Job Summary The Medical Science Liaison (MSL) Gastroenterology serves as a scientific expert and trusted partner to external healthcare stakeholders, with a strong focus on gastroenterology and inflammatory bowel disease (IBD) . The role is responsible for advancing medical education, strengthening nursing and patient engagement, supporting field-based scientific activities, and ensuring effective crossfunctional collaboration, particularly around scientific congresses and medical education initiatives. [. .. ] initiatives and field responsibilities, while balancing administrative duties and project responsibilities. Leverages knowledge of standards of care and Janssen company/ investigator sponsored clinical trials and competitor landscape to facilitate external-internal research communication. Engages with external investigators regarding unsolicited research inquiries and act as liaison to R D, Medical Affairs and operations teams. Provides clinical trial support to identify potential sites, resolve issues with enrolled sites, and participate in meetings as appropriate, including site initiation visits and investigator launch meetings. Qualifications [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Data Science Lead 1
• Mettmann, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] the ongoing operations of advanced analytics solutions to ensure that models continue to work and scale them up with additional demand and applications. You will serve as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the subject matter expert for Advanced Analytics/ AI capabilities in support of business needs within Patient Solutions and Patient Evidence. Who youll work with You will co-create with Integrated Insights Leads from early asset and late stage (Phase 0-3) teams, Real world evidence teams, Translational Medicine and Bioinformatics, Clinical operations, clinical recruitment, and asset teams, new product planning teams, Commercial teams, Medical Affairs, Market Access, Finance, and IT. Externally, you will work with data and analytics vendors and partners. What youll do Analytics Leadership: Provide clear expertise for opportunities to leverage advanced analytics, especially where they [. .. ] the conduct of advanced analytics studies in a collaborative manner ensuring that the study methodology is appropriate to deliver reliable results. Improve the teams partnership with, and impact on, key internal (UCB) and external stakeholders within the specific area of focus by: developing and executing a communication and collaboration plan with key UCB stakeholders increasing personal and the Advanced Analytics teams knowledge of the business by ensuring that she/ he and each team member has direct interaction with patients and/or [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Product Artwork Automation Technical Lead
• Schaffhausen
Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise in Innovative Medicine and Med Tech 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 jnj. com As guided by Our Credo, Johnson Johnson is responsible to our employees who work with us [. .. ] in supporting and driving technical innovation and automation within our Product Artwork (PA) team, ensuring operational excellence and futurereadiness. The selected candidate will serve as a technical and automation subjectmatter expert (SME) , driving artwork automation initiatives, resolving complex technical artwork issues and challenges, and partnering with crossfunctional teams to deliver efficient, scalable solutions. This role is central to coordinating and troubleshooting all technical aspects of product artwork while embracing change and managing complexity. The candidate will foster strong collaboration and [. .. ] is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https:/ / , internal employees contact Ask GS to be directed to your accommodation resource. Required Skills: Coaching, Critical Thinking, Detail Oriented, EHS Compliance, Engineering, Good Manufacturing Practices (GMP) , Lean Supply Chain Management, Package and Labeling Regulations, Package Management, Process Improvements, Product Packaging Design, Quality Assurance (QA) , Safety Oriented, Science, Technology, Engineering, and [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Internal Medicine expert pro Jahr?
Als Internal Medicine expert verdient man zwischen EUR 80.000,- bis EUR 130.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Internal Medicine Expert Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 84 offene Stellenanzeigen für Internal Medicine Expert Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Internal Medicine Expert Jobs?
Aktuell suchen 30 Unternehmen nach Bewerbern für Internal Medicine Expert Jobs.
Welche Unternehmen suchen nach Bewerbern für Internal Medicine Expert Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Internal Medicine Expert Stellenangebote:
- PAUL HARTMANN AG (8 Jobs)
- Siemens Healthineers AG (3 Jobs)
- NVision Imaging Technologies (3 Jobs)
- Fresenius Medical Care Deutschland GmbH (1 Job)
- United Nations (1 Job)
In welchen Bundesländern werden die meisten Internal Medicine Expert Jobs angeboten?
Die meisten Stellenanzeigen für Internal Medicine Expert Jobs werden derzeit in Baden-Württemberg (13 Jobs), Bayern (11 Jobs) und Niedersachsen (10 Jobs) angeboten.
Zu welchem Berufsfeld gehören Internal Medicine Expert Jobs?
Internal Medicine Expert Jobs gehören zum Berufsfeld Ärzte.
