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We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics..... click apply for full job details

Digital Health Leader (M/F/X) Basel Headquarter Apply At Roche, over 90,000 people across 150 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, and on seeing each other's differences as an advantage. To innovate healthcare, Roche has ambitious plans to keep learning and growing - and is seeking people who have the same goals for themselves. The position: The Digital Health Leader is a subject matter specialist for Digital Health and provides subject matter expertise to the Digital Health initiatives and business processes for the assigned programs within Medical Affairs covering the following areas: Patient Identification - improved screening and stratification of patient populations Disease Management - clinical grade information at the point of care informing decision-making Outcomes & Value - Improved characterization of the patient experience Develops standard processes, guidelines, and tools to accomplish the Digital Health programs, and ensures that they are performed in compliant and strategic manner Provides expertise and innovation for Digital Health and drives implementation of the Digital Health programs across PDMA (Product Development Medical Affairs) Are you ready to apply but have additional questions? Please check our FAQs and videos on careers.roche.ch/faq. We look forward to your application! Roche is an equal opportunity employer. Medical Affairs, Medical Affairs > Medical Information/Scientific Affairs Apply Posted Yesterday Full time 20145 About Us We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. We are proud of who we are, what we do, and how we do it. We are many, working as one across functions, across companies, and across the world. We are Roche . Follow Us In this role: You will contribute to the strategy by: Contributing to the Digital Health (DH) 5 years strategy for PDMA, anticipates and identify business needs and priorities for the assigned programs Developing the businesses processes in partnership with Digital Health Leadership Council, Digital Excellence, Regions and Legal Providing strategic input to the DH team and partners across the organisation to align priorities and goals for DH programs Being responsible for the Digital Health PDMA programs within TAs in partnership with PHC COE, REDs, US, Affiliates etc.) Defining the Digital Health success metrics, reports and processes to measure the effectiveness of Digital Health programs for the assigned TAs and deliver output as appropriate to governance bodies Providing subject matter expertise and insight in Digital Health for the medical network You will be in charge of: Defining, improving and developing business and funding processes incl regulatory and compliance aspects and technology infrastructure striving for excellence in Digital Health implementation Driving the implementation of Digital Health programs for the assigned therapeutic areas through new business model for PDMA and affiliates Driving effective utilization and further development of Digital Health knowledge tools and platforms to achieve standard methodology in Digital Health planning and cross-functional coordination Leading the strategic planning of Digital Health solutions for the assigned Therapeutic Areas as part of the medical planning process and ensure implementation for the assigned Therapeutic Areas in close collaboration with Global Medical Teams Defines the Digital Health agency and technology providers identification and management approach for the assigned programs, in collaboration with procurement and Healthcare Technology Office Provides key subject matter expertise to build the Digital Health competency and required skills for PDMA in collaboration with Medical Excellence Maintain the PDMA Digital Health content & education in PDMA You will act as a strategic collaborator: Developing a close collaboration with the key partners on the program, including Disease Area Heads, Steering Comitee Head /GL SC and Global Medical Team Leaders to understand their needs, strategic priorities, and pain points, as well as gather insights Ensuring efficient communication and working relationship with internal partners (e.g. Medical Affairs, HTO, Digital Excellence, Strategic Innovation, Regulatory, Compliance, IT, Legal etc.), US Medical Affairs, Affiliates/Regions and external technology providers Developing external collaborations in the Digital Health space to advance our PDMA strategic Digital Health portfolio Contributing to the creation of a Digital Health community across the affiliates and Global and fosters experience sharing You have the opportunity to work in compliance: Working with Regulatory, Legal, Safety and Compliance to assess gaps and needs on business and compliance processes related to Digital Health activities for PDMA and affiliates Taking responsibility for acting in line with legal, regulatory and company standards and codes of practice (such as Roche Code of Conduct and any other Roche directives and guidelines) Completing all required training modules as a priority and is responsible for all team members to act similarly We are looking for the following qualifications: Professional and Technical Requirements: You hold a Bachelor's degree in science or biology related field An advanced degree, (e.g. MBA, PhD, PharmD, MD, Engineer) is strongly preferred You have expertise in Digital Health and preferably in Medical Affairs You bring the following Technical Competencies: Ability to demonstrate Roche Values and Leadership Commitments Digital Health technical ad regulatory expertise and capability building Good organization, prioritization and planning skills Good influencing and negotiation skills Mentoring and training skills Good communication & presentation skills Very good project management skills: can prioritize multiple tasks and goals to ensure timely, on-target and within-budget accomplishment Good interpersonal and partnering skills: has validated abilities to work effectively and efficiently in cross-functional and matrix teams Financial acumen sufficient for effective and efficient management of budget and other resources Ability to promote and role-model integrity and compliance with internal and external regulations Your experience and skills involve: A minimum of 7 years of professional experience in the pharmaceutical/ biotechnology industry or related experience (preferably in positions related to Digital Health) Experience with key aspects of Digital Health activities, and healthcare professional (HCP) and patient/ patient groups interactions strongly preferred Experience in successfully handling agencies and working with technology providers Experience as a successful conclusive leader in a multi-functional environment Shown ability to work in a matrix setting Relevant scientific knowledge Pharmaceutical industry knowledge and understanding /experience with regulatory requirements and commercialization processes Appreciates the diversity of working in a multi-functional and multi-cultural environment Fluency in written and spoken English Digital Health solutions skills

We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics..... click apply for full job details

Für über 500 verschiedene Berufe suchen wir motivierte Mitarbeiter. Und das in ganz Deutschland. Ob erfahrene Profis oder Berufsstarter - wir bieten zahlreiche Einstiegs- und Weiterbildungsmöglichkeiten. Zum nächstmöglichen Zeitpunkt suchen wir Dich als Fachkraft für Lagerlogistik/ Materialwirtschaft (w/m/d) für die DB Fernverkehr AG am Standort Basel. Deine Aufgaben: Warenannahme..... klicken sie bewerben, für die volle Stellenbeschreibung

We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics..... click apply for full job details

We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics..... click apply for full job details

Senior Regulatory China Advisor The Senior Regulatory China Advisor is an expert on the evolving China CMC regulatory requirements. The role is impact-critical to the company; having strategic involvement across product portfolio for the second largest Roche Market. In this job you will be responsible for the development of China's innovative regulatory strategies across the Roche Pharma Portfolio and throughout the product lifecycle. You will be working closely with the China Regulatory Group on prioritizing key CMC issues for policy outreach and shaping the external regulatory environment. In addition you will ensure up-to-date China requirements are maintained, communicated and integrated into project team's work plans, and aligned with project teams, Pharma Development Regulatory (PDR) China and the Regulatory Policy Group. You will: Lead and be accountable for the development, communication and execution of the China CMC Regulatory Strategy for products across the portfolio to: Ensure that China requirements are incorporated in product planning strategies using a risk-based approaches' that minimizes China specific studies Drive acceleration in filing and approval of timelines to maximize early access of Roche medicines in China using innovative regulatory approaches Work across platforms in Pharma Technical Operations Regulatory (PTR) to ensure that the China strategy is inclusive and informed by the overall global CMC development strategies and priorities Facilitate product lifecycle management to ensure continuous supply to China Partner effectively and advise internal teams on optimized China regulatory strategies for development and commercial products, ensuring sound regulatory and science-based approaches Partner effectively with China Pharma Development Regulatory Group based in Beijing and Shanghai to facilitate local execution of regulatory submissions and strategies Establish an internal business process for including updated China regulatory requirements in PTR country requirements database, and proactively communicate such requirements to key stakeholders within Pharma Technical Operations Actively engage in China CMC regulatory policy activities by prioritizing CMC topics of key importance to drive convergence of China regulatory requirements with international standards, and by coordinating educational outreach to China authorities, engaging appropriate global technical experts Build and maintain relationships based on trust and respect with key China health authorities including NMPA, CDE, NIFDC and Chinese Pharmacopoeias Gather, assess and timely communicate regulatory intelligence on China trends and relevant changes in the evolving regulatory environment to key stakeholders Who you are You're someone who wants to influence your own development. You're looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point. You preferably have a Master's Degree in life science disciplines; a Post Graduate Degree is a plus. Bachelor's Degree plus appropriate working experience in pharmaceutical industry is also appropriate. You bring a minimum of 10 years of experience in Regulatory Operations and/or Policy, with a significant focus on China related activities. An in-depth understanding of China's CMC regulatory requirements across product lifecycle is a must, and you are broadly recognized as an expert in the field with established credibility across the industry. In addition you bring the following skills and competencies: Proven ability to develop innovative regulatory strategies and to adapt evolving regulatory requirements to maximize business value; you challenge the status quo to drive innovation Proven ability to build and maintain strong relationships with relevant Health Authorities in China; you have excellent collaboration skills in a multi-cultural environment and the ability to work collaboratively with international teams and with external industry/scientific associations Demonstrated capabilities to work effectively in a global matrix environment, while keeping management informed and consulted as needed Strong verbal and written communication as well as presentation skills: you exhibit a professional maturity, confidence and competence Ability to think and act decisively and effectively, and to quickly summarize complex issues and conclusions so as to expedite agreements and decision-making Fluency in Mandarin Chinese and in English, both written and spoken is mandatory

We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics..... click apply for full job details

We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics..... click apply for full job details

We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics..... click apply for full job details

We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics..... click apply for full job details

Die HMS Networks Gruppe ist der international führende Anbieter im Bereich der industriellen Datenkommunikationslösungen und beschäftigt mehr als 520 Mitarbeiter in 14 Ländern weltweit. Innerhalb der HMS Gruppe ist die HMS Industrial Networks GmbH mit rund 50 Mitarbeitern verant­wort­lich für den Vertrieb, das Marketing und den technischen Service aller HMS Marken in Mitteleuropa..... klicken sie bewerben, für die volle Stellenbeschreibung

Die Celonic AG ist ein international tätiges und schnell wachsendes Dienstleistungsunternehmen im Bereich der Biotechnologie. Als CDMO bieten wir Services zur Produktion von Biopharmazeutika an, beginnend bei der Zelllinienentwicklung bis zur GMP-gerechten Herstellung von therapeutischen Proteinen für klinische Phasen und die Marktversorgung. Wir sind empathisch, effizient und..... klicken sie bewerben, für die volle Stellenbeschreibung

Studydrive ist mit mehr als 750.000 Nutzern Europas größte Studierendenplattform. Hier findest du neben den besten Lerninhalten eine aktive und hilfsbereite Community, in der keine Frage offen bleibt! Bis heute wurden mehr als 300.000 Lernmaterialien miteinander geteilt und über 1.000.000 Fragen beantwortet. Dadurch wird das Studium für alle leichter und erfolgreicher! Studieren..... klicken sie bewerben, für die volle Stellenbeschreibung