Gehaltsübersicht für Global Medical Leader in Basel-Stadt

Medical Science Liaison – Team Build – Oncology Immunotherapy As part of an exciting immuno-oncology team build across the EU comprising commercial and medical heads, IQVIA’s international medical affairs team is recruiting for 6 newly created MSL positions – based in Belgium, Portugal, Sweden, Denmark, Switzerland and Austria. Our client is a leading biotechnology company that invents, develops, and commercializes life-transforming medicines for people with serious diseases; their therapy areas of focus include rare diseases, infectious diseases, haematological conditions, and various cancers. This oncology focused MSL team will be responsible for providing field based medical affairs support on a national level to HCPs, and local commercial colleagues, as the company expands into new European markets; working with an EMA approved, PD-1 immune checkpoint inhibitor currently indicated in cutaneous squamous cell carcinoma (CSCC), basal cell carcinoma (BCC) and non-small cell lung cancer (NSCLC) – with new indications undergoing clinical development and other exciting oncology assets in the pipeline at phase III - this is an exciting time to join an ambitious, growing company. Requirements: We are looking for candidates with very specific skills and profile: Must already be working in a similar pharma industry MSL post in the country in question Deep oncology therapy area knowledge essential, ideally within immunotherapy, melanoma, or lung cancer Prior experience of working with prelaunch products would be advantageous Outstanding communication and engagement skills Strong scientific background – ideally PhD, PharmD, MD or MSc Eligible to work in this country full time Fluency in local language and English are essential Willingness to travel nationally as required Full driving license. Benefits: Excellent salary, bonus, and benefits package We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, colour, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity, and intellectual courage every step of the way. Learn more at jobs.iqvia.com . IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes. To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.Über das Unternehmen:iqvia

Medical Director / Rheumatology, Autoimmune Translational MedicineJob ID 385923BR Nov 01, 2023 Switzerland About the Role 30 million! That is the estimated number of patients worldwide suffering from inflammatory arthritis. Join Novartis to help find the right drugs that transform and improve patients' lives all around the world. You will join an international team of clinicians and scientists making significant impact on autoimmune diseases with high unmet medical need, taking new medicines into early-stage clinical trials: in many cases you will be the first to witness the effectiveness of a new medicine that may transform the lives of millions. Your medical and scientific leadership / expertise will significantly impacts the Novartis autoimmune drug development pipeline. Go to https://www.novartis.com/our-science and scroll to the Autoimmunity research area and Translational Medicine area for more information Your responsibilities will include:• Medical / scientific contributor and leader of complex global cross-functional teams. Our successful drug discovery and development environment has close collaboration across Research, Clinical Research and Development.• Major initiator of the Proof-of-Concept strategy and the early Clinical Development Plan. Develop and implement strategies for efficient, high value management of drug development projects leading to clinical Proof-of-Concept and competitiveness of compounds• Develop and implement disease area and biomarker strategies: contribute effectively to the preclinical and clinical Disease Area strategies, project-specific Biomarker strategy, innovative target identification and in-licensing efforts resulting in a high quality preclinical and clinical portfolio• Ensure full implementation of studies during the Proof-of-Concept phase by providing medical and scientific leadership and expertise to all line functions on the project team, and direct or supervisory medical support for all pharmacokinetic studies• Translational Medicine representative to Health Authorities in matters and meetings that focus on early exploratory development: negotiate effectively with Health Authority representatives on all aspects of Translational Medicine and obtain results favorable to Novartis. Translational Medicine representative to Translational Medicine/medically related experts and organizations, advancing the interests of Novartis by your knowledge, style and personal skill and enhancing the position of Novartis with these individuals and groups• Contribute senior expertise to Research in support of target identification, selection, target validation and preclinical development of compounds. Review and evaluates cross-Disease Area activities at and beyond the early compound optimization stage. Provide clinical context and help design optimal preclinical studies• Evaluate clinical centers and foster communication with crucial collaborating investigators. Interact effectively with external medical and non-medical leaders and be an internal Novartis expert leader in your scientific and clinical subspecialty field. Matrix people responsibility per project: 5-8 cross-functional members from Translational Medicine plus other line functions per project team Impact of this role?• Design and implementation of early Clinical Development Plan and studies according to the Integrated Development Plan / Clinical Development Plan / Clinical Pharmacology Plan enabling efficient and rational decision-making, high probability of fast drug registration, favorable drug label and high competitiveness of compounds• This role has a key impact on the entire Novartis pipeline, transitioning programs from preclinical through early clinical and ultimately to full development via the Proof of Concept mechanism, and driving the program after Proof of Concept by delivering key Profiling data to support regulatory submissions• As a recognized expert in your field, you drive project team clinical strategies and bring global credibility across various Novartis Institutes and Divisions as well as country organizations Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements This position is written for Director - we can hire Associate Director for those with careers that include less established science / clinical study experience. We support International family relocation and integration support to Switzerland. What you’ll bring to the role:• MD and Board certified Rheumatologist (or similar relevant sub-specialty clinical training with directly relevant patient experience) with PhD-level basic science. A completed relevant postdoctoral fellowship is strongly preferred• Advanced / business-level / fluent English (oral and written)• Recognized for your medical expertise: an experienced Clinician treating relevant patient groups at an academic medical center or private medical practice group• Recognized for your scientific expertise: respected by colleagues internally and externally, you’ve made significant contributions to your field and created / established new concepts; you have a record of high quality publications in international scientific journals• Experience designing and conducting early phase clinical trials including for inflammatory arthritis: either from pharma/biotech, a senior CRO role where you were responsible for the medical relationship and studies with Sponsors, or from a relevant academic medical center with co-PI ideally also PI clinical trial experience. 5+ years trial experience particularly in inflammatory arthritis preferred• You are used to working independently and within teams including autoimmune disease research scientists and non-scientists on study planning and execution, demonstrating competence in a broad range of project and more strategic planning skills and leading complex cross-functional/matrix project teams Your behavioural characteristics• Demonstrated passion for treating patients and science• Strategic thinker: you have created major innovations, networked with and influenced external medical leaders with your clear and logical presentation of complex strategic issues• Results-driven self-starter and decision taker• Strong cooperative team player, flexible in a changing environment• Good planning, prioritisation, problem solving and organisational skills• Resilient, energetic and enthusiastic; responding constructively to challenging new ideas and input ABOUT TRANSLATIONAL MEDICINE:Translational Medicine is a global group of scientists and physicians working at the pre-clinical and early clinical stage of drug discovery. Our Physician-Scientists drive innovative and cutting-edge science through the selection, profiling and effective global development of successful medicines, integrating clinical science into the discovery and preclinical development phase. Our Translational Medicine concepts are driven by medical needs of patients and the concept of personalized medicine, tailoring the drug, dose and dosing regimen to the patient so the clinical response is optimal in efficacy and safety. We focus from identification of drug targets (molecular pathways relevant to disease) up to the completion of Proof of Concept (Phase IIa studies). Our Translational Medicine Experts are part of preclinical project teams in all drug discovery phases and help design the pathway for First in Human studies (healthy volunteer) that bridge to studies in the patient population. They have the comprehensive responsibility for designing and executing the early clinical drug development phase with a project team including research, biomarkers, biostatistics, modeling & simulation, toxicology, technical experts and clinical trial teams. Why Novartis?766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Division Biomedical Research Business Unit Translational Medicine Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Global Head of Immunology Early DevelopmentThe Position In Roche’s Pharmaceutical Research and Early Development organization (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs. At pRED, we are united by our mission to transform science into medicines. Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed. You are a member of the Immunology leadership team, reporting to the pRED Global Head of Immunology. The focus of Immunology Early Development is to advance early clinical immunology development programs from preclinical studies through proof of concept and dose ranging phase 2 studies. This role is a key enabler in delivering on the clinical pipeline as well as the overall ambitions of the organization. Your main responsibilities You are responsible for the strategy of the immunology early clinical development portfolio and pipeline, and mentor, develop, guide, and serve as the leader for the clinical scientists, medical directors, and project team leaders. You work with the clinical phase project teams to ensure that clinical and clinical biomarker development plans, objectives, and deliverables are consistently accomplished on-time and on-target for assigned projects. You chair the Development Review Committee and provide key feedback and guidance on project strategy and plans and represent Immunology on the pRED Early Strategic Portfolio Committee. You serve as a core member of the pRED Immunology leadership team to build disease area strategy, discovery and development strategy, and operational excellence You explore and implement collaborations with industry and academia to increase understanding of disease biology, facilitate the prosecution of portfolio in early clinical development and build our clinical portfolio. You liaise with Roche Pharma Late Stage Development, Global Product Strategy, Regulatory and Clinical Operations, as well as other Roche Research and Discovery Units in discussions around disease strategy, discovery and development strategy, and operational excellence. Your profile With a MD or MD/PhD, you bring at least 5-10 yrs of experience in pharmaceutical research and development with a broad understanding of immune-mediated diseases, clinical trial design and methodology as well as biomarkers and diagnostics. You can ideally demonstrate a solid track record of successfully translating molecules from discovery into the clinical setting as well as an understanding of regulatory, payer, and commercial issues in the pharmaceutical industry. Your leadership has been demonstrated by an ability to work with peers across a matrix organization to deliver on common goals. You inspire people to think bold, to innovate, collaborate and create great outcomes that matter for our patients and customers. You are a leader who creates and communicates a clear strategic vision for the team and the organization. This includes monitoring and reassessing strategic priorities, articulating long-term opportunities/threats, evaluating options, and building clear paths to success You understand how to make difficult decisions and will be able to focus on key priorities and delivery toward goals and have the ability to empower teams, inspiring and creating a strong sense of team spirit in the organization. You help everyone on your team to build the skills and mindset they need to succeed. Our commitment Roche commits to recognising talent and aptitude. We prioritise encouraging and supporting our employees on their personal journeys by providing a safe, creative space to help them reflect, make decisions and grow in their career. We are confident that we find the most innovative solutions by gaining different perspectives, asking and answering hard questions, and challenging the status quo. Roche embraces diversity and equal opportunity in a serious yet enthusiastic way; we are devoted to building a team that represents a range of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be. Who we are At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity. Basel is the headquarters of the Roche Group and one of its most important centres of pharmaceutical research. Over 10,700 employees from over 100 countries come together at our Basel/Kaiseraugst site, which is one of Roche`s largest sites. Read more. Besides extensive development and training opportunities, we offer flexible working options, 18 weeks of maternity leave and 10 weeks of gender independent partnership leave. Our employees also benefit from multiple services on site such as child-care facilities, medical services, restaurants and cafeterias, as well as various employee events. We believe in the power of diversity and inclusion, and strive to identify and create opportunities that enable all people to bring their unique selves to Roche. Roche is an Equal Opportunity Employer.

Global Head of Immunology Early DevelopmentThe Position In Roche’s Pharmaceutical Research and Early Development organization (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs. At pRED, we are united by our mission to transform science into medicines. Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed. You are a member of the Immunology leadership team, reporting to the pRED Global Head of Immunology. The focus of Immunology Early Development is to advance early clinical immunology development programs from preclinical studies through proof of concept and dose ranging phase 2 studies. This role is a key enabler in delivering on the clinical pipeline as well as the overall ambitions of the organization. Your main responsibilities You are responsible for the strategy of the immunology early clinical development portfolio and pipeline, and mentor, develop, guide, and serve as the leader for the clinical scientists, medical directors, and project team leaders. You work with the clinical phase project teams to ensure that clinical and clinical biomarker development plans, objectives, and deliverables are consistently accomplished on-time and on-target for assigned projects. You chair the Development Review Committee and provide key feedback and guidance on project strategy and plans and represent Immunology on the pRED Early Strategic Portfolio Committee. You serve as a core member of the pRED Immunology leadership team to build disease area strategy, discovery and development strategy, and operational excellence You explore and implement collaborations with industry and academia to increase understanding of disease biology, facilitate the prosecution of portfolio in early clinical development and build our clinical portfolio. You liaise with Roche Pharma Late Stage Development, Global Product Strategy, Regulatory and Clinical Operations, as well as other Roche Research and Discovery Units in discussions around disease strategy, discovery and development strategy, and operational excellence. Your profile With a MD or MD/PhD, you bring at least 5-10 years of experience in pharmaceutical research and development with a broad understanding of immune-mediated diseases, clinical trial design and methodology as well as biomarkers and diagnostics. You can ideally demonstrate a solid track record of successfully translating molecules from discovery into the clinical setting as well as an understanding of regulatory, payer, and commercial issues in the pharmaceutical industry. Your leadership has been demonstrated by an ability to work with peers across a matrix organization to deliver on common goals. You inspire people to think bold, to innovate, collaborate and create great outcomes that matter for our patients and customers. You are a leader who creates and communicates a clear strategic vision for the team and the organization. This includes monitoring and reassessing strategic priorities, articulating long-term opportunities/threats, evaluating options, and building clear paths to success You understand how to make difficult decisions and will be able to focus on key priorities and delivery toward goals and have the ability to empower teams, inspiring and creating a strong sense of team spirit in the organization. You help everyone on your team to build the skills and mindset they need to succeed. Our commitment Roche commits to recognising talent and aptitude. We prioritise encouraging and supporting our employees on their personal journeys by providing a safe, creative space to help them reflect, make decisions and grow in their career. We are confident that we find the most innovative solutions by gaining different perspectives, asking and answering hard questions, and challenging the status quo. Roche embraces diversity and equal opportunity in a serious yet enthusiastic way; we are devoted to building a team that represents a range of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be. Who we are At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity. Basel is the headquarters of the Roche Group and one of its most important centres of pharmaceutical research. Over 10,700 employees from over 100 countries come together at our Basel/Kaiseraugst site, which is one of Roche`s largest sites. Read more. Besides extensive development and training opportunities, we offer flexible working options, 18 weeks of maternity leave and 10 weeks of gender independent partnership leave. Our employees also benefit from multiple services on site such as child-care facilities, medical services, restaurants and cafeterias, as well as various employee events. We believe in the power of diversity and inclusion, and strive to identify and create opportunities that enable all people to bring their unique selves to Roche. Roche is an Equal Opportunity Employer.

Pre-Fillable Syringe Engineer (m/w/d) Jobdescription For our client, an international pharmaceutical company based in Basel, we are looking for an Pre-Fillable Syringe Engineer. The perfect candidate has minimum 5 years experience in drug delivery device development, pref. pre-filled syringes, in a GMP regulated environment. Experience with Quality System Regulation (QSR), Design Control or similar working practices is required and the person needs to have a sound knowledge of legislation, regulation, industry standards and guidance within the area of combination products and medical devices. General Information: Start date: 01.03.2024 Latest Start Date: 01.06.2024 Planned duration: unlimited Workplace: Basel Workload: 100% Home Office: max. 40% Team: 14 Team members Working hours: Standard Tasks & Responsibilities: Serving as primary packaging expert on technical development teams to provide the best-in-class containers and drug delivery devices for our medicines Author design control documentation (Design Development Plans, User Requirements Specifications, Design Inputs, Design Outputs, Design Verification Plans and DHF creation/maintenance DHF), conformity assessments and risk management documentation Application of theoretical engineering knowledge, to establish robust technical product requirements, and develop engineering design solutions to assure drug containers and devices maintain the required level of performance throughout the life of the product Support project leader to successfully bring drug-device combination products and medical devices to the market Apply knowledge of the regulatory landscape to ensure standard compliant designs (e.g. ISO 13485, 21CFR820, ISO14971 and 21 CFR 820.30) The role will require considerable cross-functional interaction within the department and with partner functions including Device Quality, Device Regulatory, Global Product Strategy, and Pharmaceutical & Analytical Development, as well as with external suppliers Must Haves: University level education (engineering / science degree or related discipline) At least 5 years proven track record in pharmaceutical, biomedical, material science or different GMP related field At least 5 years experience within drug delivery device development Experience of working in Quality System Regulation (QSR), Design Control or similar working practices Sound knowledge of legislation, regulation, industry standards and guidance within the area of combination products and medical devices with experience with Health Authority interactions Demonstrable knowledge of the following: drug delivery devices, primary packaging, drug container interactions, parenteral drug delivery Demonstrable knowledge of the following: risk assessment, tolerance analysis, statistical techniques, process capability, manufacturing processes and transport studies and validation Excellent command of English language and proficiency in German preferable Excellent documentation, presentation and interpersonal communication skills Luca Furler

Pre-Fillable Syringe Engineer For our international medical partner, F. Hoffmann-La Roche Ltd. in Basel, we are looking for a qualified and motivated Pre-Fillable Syringe Engineer for a temporary contract of 12 months. The Device and Packaging Development Department within Roche Pharma Technical Development is responsible for the development and support of drug delivery devices for the product portfolio. The activities span a range of engineering disciplines from the requirements definition phase, development through to commercialization. Roche is recruiting for a Pre-Fillable Syringe Engineer to support the development and maintenance of drug delivery devices (e.g. Prefilled Syringes with Needle Safety Devices, Autoinjectors, high-volume Patch-injectors). Tasks Serving as primary packaging expert on technical development teams to provide the best-in-class containers and drug delivery devices for our medicines Author design control documentation (Design Development Plans, User Requirements Specifications, Design Inputs, Design Outputs, Design Verification Plans and DHF creation/maintenance DHF), conformity assessments and risk management documentation Application of theoretical engineering knowledge, to establish robust technical product requirements, and develop engineering design solutions to assure drug containers and devices maintain the required level of performance throughout the life of the product Support project leader to successfully bring drug-device combination products and medical devices to the market Apply knowledge of the regulatory landscape to ensure standard compliant designs (e.g. ISO 13485, 21CFR820, ISO14971 and 21 CFR 820.30) The role will require considerable cross-functional interaction within the department and with partner functions including Device Quality, Device Regulatory, Global Product Strategy, and Pharmaceutical & Analytical Development, as well as with external suppliers Must Haves University level education (engineering / science degree or related discipline) At least 5 years proven track record in pharmaceutical, biomedical, material science or different GMP related field At least 5 years experience within drug delivery device development Experience of working in Quality System Regulation (QSR), Design Control or similar working practices Sound knowledge of legislation, regulation, industry standards and guidance within the area of combination products and medical devices with experience with Health Authority interactions Demonstrable knowledge of the following: drug delivery devices, primary packaging, drug container interactions, parenteral drug delivery Demonstrable knowledge of the following: risk assessment, tolerance analysis, statistical techniques, process capability, manufacturing processes and transport studies and validation Excellent command of English language and proficiency in German preferable Excellent documentation, presentation and interpersonal communication skills Are you interested? Do not hesitate and submit your complete application documents online today. We also process applications by post, but will not return them for administrative reasons. We look forward to hearing from you! Wir wertschätzen Vielfalt und begrüssen daher alle Bewerbungen - unabhängig von Geschlecht, sozialer Herkunft, Religion, Alter und Identität. Zur leichteren Lesbarkeit und besseren Verständlichkeit verwenden wir nur eine Gender-Form. Selbstverständlich sind im jeweiligen Kontext alle Genderformen gleichermassen gemeint. Kontakt Adnan Ferizi Arbeitsort Basel Pensum 100% Position Mitarbeiter Branche Elektro + Mechanik

Responsibilities• Writes clear and concise clinical submission documents, including clinical study reports, protocols, clinical overviews, investigator brochures, and summary documents; experience with late-stage health authority responses is a plus.• Contributes to project plan concerning timelines as well as organization and table layout for a specific document.• Ensures that documents meet regulations, and the key messages as defined by the team are clearly and adequately represented.• Review and edit documents for consistency, progression, structure, and grammar.• Review statistical analysis plans and incorporate into clinical study reportsor submission documents, as applicable.• Drive the document preparation process, manage timelines, receive, and review primary statistical output, draft, and distribute document for review, compile comments and edits, lead comment resolution meetings independently.• Participate in team and client meetings as requested• Deliverables above plus able to work independently on a range of complex clinical documents• Interprets, summarizes, and presents statistical and medical information to ensure accuracy of content in highly complex document types independently• Resolves complex problems independentlyEDUCATION AND EXPERIENCE• At least 8(PhD)-10(Masters) years of regulatory medical writing experience in the pharmaceutical industry.•Extensive medical writing experience inclusive of clinical study documents and global clinical regulatory submissions.• Extensive authoring experience across multiple TAs in both early and late development programs.• Experience authoring Health Authority responses is required.• Strong project management skills required.• Ability to understand and interpret clinical and scientific data; ability to present results in an understandable manner to a variety of audiences.• Knowledge of current requirements and guidelines applicable to submission documents.• Excellent writing skills.• Excellent interpersonal and oral communication skills.• Strong knowledge of MS Word and Outlook, some knowledge of Excel and PowerPoint.• Project management and organizational skills required including ability to manage timelines and prioritize multiple projects.IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.comIQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.EEO Minorities/Females/Protected Veterans/DisabledÜber das Unternehmen:IQVIA

Spatial Biology Matrix LeadThe Position In Roche’s Pharmaceutical Research and Early Development organization (pRED ), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs. At pRED, we are united by our mission to transform science into medicines. Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed. 360 Labs Initiative at a Glance The 360 Labs are a new capability that is currently being built up within the Pharmaceutical Research and Early Development organization (pRED ). The primary mission of this effort is to provide greater access and support for the use of cutting-edge biomedical research technologies by scientists across our discovery portfolio. Operating as an integrated ecosystem, the 360 Lab environment will deliver core scientific technologies, expertise and enabling activities, as well as facilitate knowledge sharing and learning experiences in close collaboration with our therapeutic areas and functions. Together, these efforts will serve to increase the speed, enhance the robustness and improve the sustainability of our exploratory research and early discovery activities. We are currently recruiting scientific professionals with varied backgrounds in Flow Cytometry, Genomics, Proteomics, Histopathology and Microscopy / Imaging. In these new roles, your collaborative mindset is as valued as your scientific expertise. The 360 Labs are by nature a hands-on, interactive workplace where face to face presence in our labs is a priority. Our ambition is to bring to life a thriving workplace environment, acting as an highly integrated ecosystem, supporting research and development, working collaboratively, and focused on fostering excellence and sustainability. Job Mission and Impact The 360 Labs Initiative is seeking a Matrix Leader for Spatial Biology. You will have a strong background in the development and application of spatial approaches (both genomics and imaging-based) to understand disease biology. You will operate as a part of a matrix team and will collaborate closely with the platform heads, lab scientists and data analysts from each of the 360 Labs technology platforms, as well as with experts from our therapeutic disease areas and functions to conceptualize and execute our spatial biology strategy to support discovery projects undertaken within the 360 Labs technology ecosystem. Your Role and Responsibilities Act as a strategic visionary, providing key guidance and oversight in the deployment and application of spatial biology approaches across the discovery research space in pRED. Serve as a key member of the 360 Labs leadership team, working closely with the Global Head, to develop a bold vision and strategy for spatial biology by close interaction with senior leaders and key stakeholders across pRED. Serve as a Matrix Leader collaborating across the 360 Labs technology ecosystem along with scientific experts from our therapeutic areas and functions to prioritize and implement innovative spatial biology strategies to enable the exploration of disease-relevant hypotheses. Work collaboratively to continually evolve our spatial biology strategy by innovating new approaches, staying up to date with the scientific literature, actively engaging with internal and external spatial biology communities, and continuously evaluating new technologies in the spatial biology space. Your Profile Required Proven track record of engagement with senior leaders and key stakeholders and leading cross-functional teams. A PhD degree in biology, chemistry, or a related field with 5 yrs professional experience in an academic setting and / or pharmaceutical industry / biotech sector. An experienced experimentalist with in-depth theoretical and hands-on knowledge in the development and application of genomics and imaging-based spatial biology assays to understand how cells organize and interact across complex tissue landscapes. Established track record of scientific accomplishments and successful collaborations documented via publications in high-impact scientific journals and presentations at international conferences. Familiarity with the bioinformatics tools and programming languages commonly used in the analyses and interpretation of spatial biology-related datasets. Strong awareness of the emerging trends and technology developments across the spatial biology space. In addition to your scientific expertise and critical technical skills we are looking for candidates who: are a strategic leader that can architect a compelling vision; serve as a coach to develop and mentor junior and senior team members; and act as a catalyst by leading by example; are curious, have a growth mindset, are resourceful and flexible in problem solving, have excellent organizational skills, can think outside the box, and have a demonstrated ability to implement new ideas in a fast-paced research environment; bring excellent written communication and presentations skills with a high fluency in English; have a keen interest in continuously building a personal network and who will thrive in a dynamic, inclusive environment which gives you full accountability for your own contributions and development; have an excellent understanding of the operations processes involved in early drug discovery & development. Your Location This position is based in Basel. Our commitment Roche commits to recognizing talent and aptitude. We prioritize encouraging and supporting our employees on their personal journeys by providing a safe, creative space to help them reflect, make decisions and grow in their career. We are confident that we find the most innovative solutions by gaining different perspectives, asking and answering hard questions, and challenging the status quo. Roche embraces diversity and equal opportunity in a serious yet enthusiastic way; we are devoted to building a team that represents a range of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be. Who we are At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity. Basel is the headquarters of the Roche Group and one of its most important centres of pharmaceutical research. Over 10,700 employees from over 100 countries come together at our Basel/Kaiseraugst site, which is one of Roche`s largest sites. Read more. Besides extensive development and training opportunities, we offer flexible working options, 18 weeks of maternity leave and 10 weeks of gender independent partnership leave. Our employees also benefit from multiple services on site such as child-care facilities, medical services, restaurants and cafeterias, as well as various employee events. We believe in the power of diversity and inclusion, and strive to identify and create opportunities that enable all people to bring their unique selves to Roche. Roche is an Equal Opportunity Employer.

Research Histopathology Platform HeadThe Position In Roche’s Pharmaceutical Research and Early Development organization (pRED ), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs. At pRED, we are united by our mission to transform science into medicines. Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed. 360 Labs Initiative at a Glance The 360 Labs are a new capability that is currently being built up within the Pharmaceutical Research and Early Development organization (pRED ). The primary mission of this effort is to provide greater access and support for the use of cutting-edge biomedical research technologies by scientists across our discovery portfolio. Operating as an integrated ecosystem, the 360 Lab environment will deliver core scientific technologies, expertise and enabling activities, as well as facilitate knowledge sharing and learning experiences in close collaboration with our therapeutic areas and functions. Together, these efforts will serve to increase the speed, enhance the robustness and improve the sustainability of our exploratory research and early discovery activities. We are currently recruiting scientific professionals with varied backgrounds in Flow Cytometry, Genomics, Proteomics, Histopathology and Microscopy / Imaging. In these new roles, your collaborative mindset is as valued as your scientific expertise. The 360 Labs are by nature a hands-on, interactive workplace where face to face presence in our labs is a priority. Our ambition is to bring to life a thriving workplace environment, acting as an highly integrated ecosystem, supporting research and development, working collaboratively, and focused on fostering excellence and sustainability. Job Mission and Impact We are offering an outstanding opportunity for a highly motivated, engaged and dynamic leader to shape the strategy of a new Research Histopathology Core Technology Platform. You will have a proven track record of engaging with senior leaders and key stakeholders and have a strong background in the histological preparation and pathological interpretation of mammalian tissues and will be a pathologist (either DVM or MD with board certification ECVP/ACVP or ABPath). You will drive the early build up and growth of the Research Histopathology Core Technology Platform and its support of discovery science within the pRED organization. Your Role and Responsibilities Act as a strategic visionary, providing key guidance and oversight in the deployment and application of histopathology approaches across the discovery research space in pRED. Serve as a key member of the 360 Labs leadership team, working closely with the Global Head, to develop a bold vision and strategy to operationalize a cutting-edge histopathology core technology platform by close interaction with senior leaders and key stakeholders. Evolve and lead a matrix team with purpose, collaborating closely with our therapeutic areas and functions to prioritize and implement sensitive and cutting-edge histopathology techniques as well as coordinate, validate and direct complex research and technology development projects to explore disease-relevant hypotheses. Drive the continued evolution of the Research Histopathology Platform by innovating new approaches, staying up to date with the scientific literature, actively engaging with internal and external histopathology communities, and continuously evaluating new technologies in the field. Your Profile Required Proven track record of engagement with senior leaders and key stakeholders and leading cross-functional teams. A pathologist (either DVM or MD) with board certification (ECVP/ACVP or ABPath) with 10 yrs professional experience in an academic setting and / or pharmaceutical industry / biotech sector, with proven effective leadership of a histopathology-focused group. An experienced experimentalist with both an in-depth theoretical and hands-on knowledge of a broad-range of histopathology approaches and novel models of animal and human disease along with their application in translational medicine. Established track record of scientific accomplishments and successful collaborations documented via publications in high-impact scientific journals and presentations at international conferences. Expert knowledge in the etiology and pathogenesis of animal disease mechanisms and processes, organ system pathology and diagnostic pathology. Awareness of, and the ability to implement novel cutting-edge approaches such as next-generation technologies in the spatial biology field. In addition to your scientific expertise and critical technical skills we are looking for candidates who: are a strategic leader that can architect a compelling vision; serve as a coach to develop and mentor junior and senior team members; and act as a catalyst by leading by example; are curious, have a growth mindset, are resourceful and flexible in problem solving, have excellent organizational skills, can think outside the box, and have a demonstrated ability to implement new ideas in a fast-paced research environment; bring excellent written communication and presentations skills with a high fluency in English; have a keen interest in continuously building a personal network and who will thrive in a dynamic, inclusive environment which gives you full accountability for your own contributions and development; have an excellent understanding of the operations processes involved in early drug discovery & development. Your Location This position is based in Basel. Our commitment Roche commits to recognizing talent and aptitude. We prioritize encouraging and supporting our employees on their personal journeys by providing a safe, creative space to help them reflect, make decisions and grow in their career. We are confident that we find the most innovative solutions by gaining different perspectives, asking and answering hard questions, and challenging the status quo. Roche embraces diversity and equal opportunity in a serious yet enthusiastic way; we are devoted to building a team that represents a range of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be. Who we are At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity. Basel is the headquarters of the Roche Group and one of its most important centres of pharmaceutical research. Over 10,700 employees from over 100 countries come together at our Basel/Kaiseraugst site, which is one of Roche`s largest sites. Read more. Besides extensive development and training opportunities, we offer flexible working options, 18 weeks of maternity leave and 10 weeks of gender independent partnership leave. Our employees also benefit from multiple services on site such as child-care facilities, medical services, restaurants and cafeterias, as well as various employee events. We believe in the power of diversity and inclusion, and strive to identify and create opportunities that enable all people to bring their unique selves to Roche. Roche is an Equal Opportunity Employer.