💼 Stellenangebote 6
Research Product Team Lead m/f/d
Job opening — Research Product Team Lead m/f/d | Bayer Consumer Care AG | Basel. In this role, you will be responsible for: • Take ownership of core responsib…
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"description": "Job opening — Research Product Team Lead m/f/d | Bayer Consumer Care AG | Basel.\n\nIn this role, you will be responsible for:\n\n• Take ownership of core responsibilities within your area of expertise\n• Collaborate with cross-functional teams to achieve shared goals\n• Maintain quality standards and adhere to internal processes\n\nWe are looking for someone with:\n\n• Relevant degree and professional experience\n• Strong communication and teamwork skills\n• Professional level of English\n\nOur benefits include:\n\n• Competitive salary package\n• Flexible working arrangements\n• Career development opportunities\n\nInterested? Submit your application today.",
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Director, Integrated Product Medical Lead (m/f/d)
Vous cherchez un emploi de Director, Integrated Product Medical Lead (m/f/d) a Basel ? Bayer Consumer Care AG recrute. At Bayer we're visionaries, driven to so…
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"description": "Vous cherchez un emploi de Director, Integrated Product Medical Lead (m/f/d) a Basel ? Bayer Consumer Care AG recrute.\n\nAt Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is nolonger a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives ofthose around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you'rehungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.\nDirector, Integrated Product Medical Lead (m/f/d)\nYOUR TASKS AND RESPONSIBILITIES\nThe Integrated Product Medical Lead (IPML) is crucial for advancing the Oncology early development portfolio. As an IPML, you create a significant impact through the successful progression of global development programs and the expansion of our pipeline. You set the vision and strategic direction for assigned programs, ensuring a medically and clinically sound end-to-end development strategy for our products across various modalities, biologies, and indications, representing the full value chain from pre-D1 up to hand-over to late-stage drug development. You build an end-to-end clinical strategy and are responsible for executing development programs on behalf of Early Clinical Development Oncology (ECDO), providing clinical-scientific leadership for one or more global development programs with full decision-making authority. Collaborating with cross-functional IPT members, you drive the creation and maintenance of a target product and target value profile to maximize the clinical success of development programs, significantly shaping the value of the product. You co-lead the incorporation of novel assets into the pipeline through supporting internal and external innovation efforts. Additionally, you play a vital role in shaping functional excellence within ECDO by driving core project, people, and innovative clinical development topics under a peer-reviewed setting, pushing the boundaries of drug development in collaboration with internal and external researchers.\nKey tasks:\n•\nAct as the clinical leader and primary clinical representative for global programs, ensuring high quality and speed of functional deliverables.\n•\nDevelop a clinical vision for addressing unmet medical needs, considering the molecule's scientific hypothesis.\n•\nAccountable for timely delivery of milestones, mitigating roadblocks, and empowered to take decisions to effectively execute the clinical strategy.\n•\nSupport preclinical evaluation and validation of new oncology assets in line with the Research and Early Development Oncology (RED ONC) strategy.\n•\nGuide preclinical asset development to enable informed clinical development, facilitating go/no-go decision making.\n•\nReview key study documents, ensuring alignment with clinical development plans and target product profiles.\n•\nProvide comprehensive knowledge of the scientific, development, and regulatory landscape to enable state-of-the-art early precision drug development.\n•\nProactively interact with academic and industry partners, health authorities, key opinion leaders, and patient advocacy groups.\n•\nLead and drive ECDO-initiated strategic initiatives in support of overall ECDO, RED-ONC, Oncology, and Bayer strategy.\n•\nIndependently lead self-empowered matrix teams, promoting a creative and innovation-friendly collaboration between clinicians and scientists.\n•\nFoster a culture of ownership and empower others, driving peer accountability across portfolio deliverables.\nWHO YOU ARE\n•\nMedical excellence: M.D. with 5+ years in direct patient care and board certification within oncology/hematology or associated subspecialties.\n•\nScientific excellence demonstrated by a track record of relevant research documented in peer-reviewed publications.\n•\nOutstanding drug development expertise with 3-5 years of parcours professionnel, including 2+ years in early drug development.\n•\nExpertise across different biologies and modalities, including small and large molecules.\n•\nRelevant global health authority interactions and current knowledge of regulatory review and responses.\n•\nAbility to independently develop a sound medical strategy and teach others to do so.\n•\nStrong communication and leadership skills, strategic thinking, and good business and external trends insights.\n•\nHigh energy with focus and vision; self-motivated with a high sense of ownership and proactive, solution-oriented approach.\n•\nFluency in English is mandatory; command of a second major European language, especially German, would be an asset.\n\nVotre prochaine etape professionnelle commence ici.",
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Translation Imaging Lead m/f/d
Bayer Consumer Care AG est a la recherche d'un(e) Translation Imaging Lead m/f/d pour son site de Basel. At Bayer we're visionaries, driven to solve the world'…
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"description": "Bayer Consumer Care AG est a la recherche d'un(e) Translation Imaging Lead m/f/d pour son site de Basel.\n\nAt Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is nolonger a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives ofthose around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you'rehungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.\nTranslation Imaging Lead m/f/d\nAt Bayer, we are dedicated to advancing oncology research through innovative imaging strategies. As a Translational Imaging Lead, you will independently drive the strategic guidance for biomarker imaging across one or more programs, focusing on drug development deliverables. Your role will ensure the use of appropriate imaging techniques from early clinical through registration phases, collaborating with cross-functional teams to enhance drug development, particularly in radioligand therapies.\nYOUR TASKS AND RESPONSIBILITIES\n•\nDrive the development of strategic guidance for biomarker imaging, ensuring oncology programs utilize appropriate imaging techniques throughout the drug development process.\n•\nAdvise on the use of imaging biomarkers and techniques in clinical trials, focusing on radiopharmaceuticals in collaboration with Radiology and external imaging CROs.\n•\nParticipate in Program Teams, providing oncology expertise to develop translation and imaging strategies.\n•\nDirect the global oncology Radiomics approach, providing expertise and leadership across the portfolio.\n•\nCoordinate all aspects of imaging delivery in synchronization with the drug R&D process, informed by a deep understanding of clinical development in oncology and state-of-the-art imaging strategies.\n•\nDevelop imaging tools to measure drug response/effectiveness through internal and external collaborations.\n•\nEnsure regulatory compliance of imaging activities and drive qualification processes.\n•\nEvaluate, interpret, and present results from imaging analyses to support decision-making.\n•\nIdentify new collaboration opportunities and manage relationships with partners to drive imaging excellence.\n•\nContribute to self-empowered matrix teams, fostering a culture of creativity and innovation, and promoting a high-performance environment.\nWHO YOU ARE\n•\nMedical doctor (MD or MD/PhD) or imaging scientist (PhD) trained in radiology, nuclear medicine, imaging physics, or image analysis with a minimum of 7 years industry parcours professionnel, or a master's degree with 9 years, or a bachelor's degree with 11 years of industry background.\n•\nProven track record in research and/or development with a focus on radiopharmaceuticals and oncology applications.\n•\nExperience with clinical and preclinical imaging in oncology drug development, including PET, SPECT, CT, bioluminescence, and MRI.\n•\nThorough understanding of imaging and clinical development in oncology, including regulatory frameworks for biomarkers.\n•\nOutstanding scientific reputation with multiple publications in peer-reviewed journals and a strong network in the academic and clinical community of imaging specialties.\n•\nExcellent interpersonal and communication skills, with fluency in English.\n\nInteressé(e) ? Postulez directement sur notre site.",
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Clinical Science Lead m/f/d
Bayer Consumer Care AG ouvre un poste de Clinical Science Lead m/f/d a Basel. At Bayer we're visionaries, driven to solve the world's toughest challenges and s…
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"description": "Bayer Consumer Care AG ouvre un poste de Clinical Science Lead m/f/d a Basel.\n\nAt Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is nolonger a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives ofthose around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you'rehungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.\nClinical Science Lead m/f/d\nAs a Clinical Scientist Lead (m/f/d), you will be a key figure in leading the clinical science perspective within global oncology development programs. You will create significant impact by safeguarding the quality and integrity of oncology studies and related medical data, optimizing decision-making, and enhancing drug development within a trial's framework. Assigned to highly complex and strategic priority clinical studies, you will provide scientific leadership to develop innovative protocol and study designs, ensuring a scientifically sound end-to-end study strategy.\nYOUR TASKS AND RESPONSIBILITIES\n•\nAct as the scientific leader and primary clinical-science representative for assigned global programs\n•\nPerform scientific oversight of oncology clinical trials, ensuring scientific integrity from concept to final report\n•\nPlan and execute data-driven decision-making focused on patient centricity, urgency, and speed\n•\nLead the development and writing of protocols and related documents, providing training with additional support\n•\nProvide expert input for clinical sections of study reports and assist in regulatory submissions\n•\nManage studies and provide scientific input to operational colleagues, external parties, and study site staff\n•\nMentor and onboard junior colleagues, fostering a culture of innovation and collaboration\n•\nPromote creative collaboration between clinicians and scientists to drive the development of a robust pipeline\nWHO YOU ARE\n•\nDegree in a health/life science-related field with initial industry experience in a pharmaceutical/biotech business; oncology expertise is a plus\n•\nOutstanding drug development expertise with knowledge of various diseases and therapeutic areas\n•\nIn-depth knowledge of GCP/ICH, FDA, EMA, and relevant regulatory guidelines\n•\nHigh energy, self-motivated, and proactive with a solution-oriented approach\n•\nFocused on outcomes, independently defining and delivering on high-impact results\n•\nStrong collaborator who encourages open discussion and values diverse perspectives\n•\nFluent in English; command of a second major European language, especially German, is an asset\n\nRejoignez Bayer Consumer Care AG et donnez un nouvel elan a votre carriere.",
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Translation Imaging Lead m/f/d
Poste a pourvoir : Translation Imaging Lead m/f/d -- Basel -- Bayer Consumer Care AG. At Bayer we're visionaries, driven to solve the world's toughest challeng…
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"description": "Poste a pourvoir : Translation Imaging Lead m/f/d -- Basel -- Bayer Consumer Care AG.\n\nAt Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is nolonger a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives ofthose around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you'rehungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.\nTranslation Imaging Lead m/f/d\nAt Bayer, we are dedicated to advancing oncology research through innovative imaging strategies. As a Translational Imaging Lead, you will independently drive the strategic guidance for biomarker imaging across one or more programs, focusing on drug development deliverables. Your role will ensure the use of appropriate imaging techniques from early clinical through registration phases, collaborating with cross-functional teams to enhance drug development, particularly in radioligand therapies.\nYOUR TASKS AND RESPONSIBILITIES\n•\nDrive the development of strategic guidance for biomarker imaging, ensuring oncology programs utilize appropriate imaging techniques throughout the drug development process.\n•\nAdvise on the use of imaging biomarkers and techniques in clinical trials, focusing on radiopharmaceuticals in collaboration with Radiology and external imaging CROs.\n•\nParticipate in Program Teams, providing oncology expertise to develop translation and imaging strategies.\n•\nDirect the global oncology Radiomics approach, providing expertise and leadership across the portfolio.\n•\nCoordinate all aspects of imaging delivery in synchronization with the drug R&D process, informed by a deep understanding of clinical development in oncology and state-of-the-art imaging strategies.\n•\nDevelop imaging tools to measure drug response/effectiveness through internal and external collaborations.\n•\nEnsure regulatory compliance of imaging activities and drive qualification processes.\n•\nEvaluate, interpret, and present results from imaging analyses to support decision-making.\n•\nIdentify new collaboration opportunities and manage relationships with partners to drive imaging excellence.\n•\nContribute to self-empowered matrix teams, fostering a culture of creativity and innovation, and promoting a high-performance environment.\nWHO YOU ARE\n•\nMedical doctor (MD or MD/PhD) or imaging scientist (PhD) trained in radiology, nuclear medicine, imaging physics, or image analysis with a minimum of 7 years industry parcours professionnel, or a master's degree with 9 years, or a bachelor's degree with 11 years of industry experience.\n•\nProven track record in research and/or development with a focus on radiopharmaceuticals and oncology applications.\n•\nExperience with clinical and preclinical imaging in oncology drug development, including PET, SPECT, CT, bioluminescence, and MRI.\n•\nThorough understanding of imaging and clinical development in oncology, including regulatory frameworks for biomarkers.\n•\nOutstanding scientific reputation with multiple publications in peer-reviewed journals and a strong network in the academic and clinical community of imaging specialties.\n•\nExcellent interpersonal and communication skills, with fluency in English.\n\nVotre prochaine etape professionnelle commence ici.",
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Director, Integrated Product Medical Lead (m/f/d)
Nouvelle opportunite : Director, Integrated Product Medical Lead (m/f/d) chez Bayer Consumer Care AG (Basel). At Bayer we're visionaries, driven to solve the w…
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"description": "Nouvelle opportunite : Director, Integrated Product Medical Lead (m/f/d) chez Bayer Consumer Care AG (Basel).\n\nAt Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is nolonger a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives ofthose around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you'rehungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.\nDirector, Integrated Product Medical Lead (m/f/d)\nYOUR TASKS AND RESPONSIBILITIES\nThe Integrated Product Medical Lead (IPML) is crucial for advancing the Oncology early development portfolio. As an IPML, you create a significant impact through the successful progression of global development programs and the expansion of our pipeline. You set the vision and strategic direction for assigned programs, ensuring a medically and clinically sound end-to-end development strategy for our products across various modalities, biologies, and indications, representing the full value chain from pre-D1 up to hand-over to late-stage drug development. You build an end-to-end clinical strategy and are responsible for executing development programs on behalf of Early Clinical Development Oncology (ECDO), providing clinical-scientific leadership for one or more global development programs with full decision-making authority. Collaborating with cross-functional IPT members, you drive the creation and maintenance of a target product and target value profile to maximize the clinical success of development programs, significantly shaping the value of the product. You co-lead the incorporation of novel assets into the pipeline through supporting internal and external innovation efforts. Additionally, you play a vital role in shaping functional excellence within ECDO by driving core project, people, and innovative clinical development topics under a peer-reviewed setting, pushing the boundaries of drug development in collaboration with internal and external researchers.\nKey tasks:\n•\nAct as the clinical leader and primary clinical representative for global programs, ensuring high quality and speed of functional deliverables.\n•\nDevelop a clinical vision for addressing unmet medical needs, considering the molecule's scientific hypothesis.\n•\nAccountable for timely delivery of milestones, mitigating roadblocks, and empowered to take decisions to effectively execute the clinical strategy.\n•\nSupport preclinical evaluation and validation of new oncology assets in line with the Research and Early Development Oncology (RED ONC) strategy.\n•\nGuide preclinical asset development to enable informed clinical development, facilitating go/no-go decision making.\n•\nReview key study documents, ensuring alignment with clinical development plans and target product profiles.\n•\nProvide comprehensive knowledge of the scientific, development, and regulatory landscape to enable state-of-the-art early precision drug development.\n•\nProactively interact with academic and industry partners, health authorities, key opinion leaders, and patient advocacy groups.\n•\nLead and drive ECDO-initiated strategic initiatives in support of overall ECDO, RED-ONC, Oncology, and Bayer strategy.\n•\nIndependently lead self-empowered matrix teams, promoting a creative and innovation-friendly collaboration between clinicians and scientists.\n•\nFoster a culture of ownership and empower others, driving peer accountability across portfolio deliverables.\nWHO YOU ARE\n•\nMedical excellence: M.D. with 5+ years in direct patient care and board certification within oncology/hematology or associated subspecialties.\n•\nScientific excellence demonstrated by a track record of relevant research documented in peer-reviewed publications.\n•\nOutstanding drug development expertise with 3-5 years of experience, including 2+ years in early drug development.\n•\nExpertise across different biologies and modalities, including small and large molecules.\n•\nRelevant global health authority interactions and current knowledge of regulatory review and responses.\n•\nAbility to independently develop a sound medical strategy and teach others to do so.\n•\nStrong communication and leadership skills, strategic thinking, and good business and external trends insights.\n•\nHigh energy with focus and vision; self-motivated with a high sense of ownership and proactive, solution-oriented approach.\n•\nFluency in English is mandatory; command of a second major European language, especially German, would be an asset.\n\nNe laissez pas passer cette offre -- postulez maintenant.",
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