Senior Manager (f/m/d) Clinical Affairs
SIEMENSErlangenUpdate time: March 9,2023
Job Description
Do you want to help create the future of healthcare? Our name, Siemens Healthineers, was selected to honor our people who dedicate their energy and passion to this cause. It reflects their pioneering spirit combined with our long history of engineering in the ever-evolving healthcare industry. We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sound interesting? Then come and join our global team as Senior Manager (f/m/d) Clinical Affairs to support our Business Areas/Lines, Business Horizontals and Technology Excellent Units in close cooperation with our country organizations in the application-oriented interpretation and implementation of global clinical requirements for in-vivo and in-vitro diagnostic medical devices. Choose the best place for your work – Within the scope of this position, it is possible, in consultation with your manager, to work mobile (within Germany) up to an average volume of 60% of the respective working hours. Your tasks and responsibilities: You guide Siemens Healthineers (SHS) Units in all clinical matters; this includes evaluation of medical devices and performance evaluation of in-vitro diagnostics (IVDs), their planning and determination of relevant data sources, systematic literature search and scientific evaluation and presentation of relevant data global post-market clinical follow-up activities, including post-market clinical trials and vigilance qualification and monitoring of clinical trial sites You support the SHS Units in the implementation of global regulations for clinical investigations, clinical studies, and performance evaluation studies establishment of clinical development strategies, planning and execution of clinical investigations/studies communication with national competent authorities, ethics committees and contract research organizations qualification and monitoring of clinical investigation/study sites You analyze global clinical regulations and establish SHS-wide provisions that detail the conduct of required clinical activities. In addition, you effectively communicate these clinical regulations to the global SHS clinical community Together with subject matter experts you identify possible improvement potentials not only in clinical affairs but also in the post market processes, develop solutions, and optimize interfaces and communication channels You provide trainings and coach SHS units and external customers e.g., in global clinical processes and communication with national competent authorities and clinical investigators. This includes creation of corresponding training concepts and training material You monitor and audit clinical investigation/study sites in accordance with ISO 14155 and support clinical investigation/study sites during an audit or inspection. You work with international industry associations and standard organizations to harmonize global clinical regulations and standards To find out more about the specific business, have a look at https://www.siemens-healthineers.com/products-services Your qualifications and experience: You have a university degree in human medicine or biology and/or equivalent qualification and experience You have several years of professional experience in a Clinical Affairs function or equivalent in the medical device/IVD industry, an academic clinical research center or a contract research organization You have profound knowledge of the regulatory requirements for medical devices and IVDs and are proficient in the most current version of clinical MDCGs (such as MDCG 2020-6 incl. relevant parts of MEDDEV 2.7/1) and ISO 14155. Ideally you have clinical expertise not only for the European Union but also for other countries such as China and the USA You can demonstrate profound knowledge and practical experience in managing clinical investigations and/or performance evaluation studies and bring experience in Post Market Clinical Follow Up You have experience in the management and monitoring of clinical trials and/or (clinical) performance evaluation studies You have gained fundamental knowledge in clinical research methodologies, including clinical investigation/study design, biostatistics, information management (e.g., use of scientific literature databases), and medical writing Preferable you can contribute already existing expertise in post-market aspects and are willing to familiarize yourself in further regulatory affairs and quality management topics Your attributes and skills: You have a goal-oriented, structured work style, are assertive and know how to use your intercultural experience to manage different cultures and personalities in international teams You enjoy teamwork and are willing to lead expert teams; your capabilities and skills for leading interdisciplinary teams have been proven Your personal strengths include entrepreneurial thinking and acting, strong motivational skills, analytical penetration, a high level of initiative as well as high resilience and flexibility You are flexible and travel to the local partners, as needed - international travel (max. 20%) With your strong communication and presentation skills in German and English you can without problems conduct trainings and workshops as well as exchange with international colleagues and partners Our global team: Siemens Healthineers is a leading global medical technology company. 66,000 dedicated colleagues in over 70 countries are driven to shape the future of 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. That’s why we invite you to take on new challenges, test your ideas, and celebrate success. Check our Careers Site at https://www.siemens-healthineers.com/de/careers As an equal opportunity employer, we welcome applications from individuals with disabilities. Wish to find out more before applying? Contact us: +49 (9131) / 17 – 1717, if you wish to discuss any initial questions with our recruitment team. The contact person handling this job ad is Simone Morgenstern. We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open. Click here to get started. Siemens Healthineers Germany was awarded the Great Place to Work® certificate. Organization: Siemens Healthineers Company: Siemens Healthcare GmbH Experience Level: Experienced Professional Full / Part time: Full-time

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