Clinical Research
Vor 3 Tagen
Your main tasks
Responsible for overseeing global clinical trials, ensuring compliance with ISO :0, the Declaration of Helsinki, and relevant national laws and regulations. This includes adherence to Articles through and Annex XV of EU Regulation 7/ (MDR), as well as adhering to clinical trial standards as governed by the Food and Drug Administration (FDA) Responsibility for adherence to budgets, timelines, milestones, and task completion of clinical trials Supervising and supporting CROs and trial centers in the preparation and conduct of clinical studies in compliance in close collaboration with medical experts and external advisors Planning, coordination and conduct of audits according to predefined audit plans and checklists at CROs and trial sites to ensure compliance with GCP guidelines, internal quality standards, study protocols and regulatory requirements Establish and maintain a constructive relationship with local & international opinion leaders, trial centers, CROs and other third parties Effective communication with internal and external stakeholders including regulatory authorities, ethics committees, CROs, investigators and advisors Contribution to the scientific evaluation and interpretation of the study results, including the preparation of reports and publications Organization and implementation of training measures for Ypsomed employees and study team members to ensure compliance with study standards and guidelines Medical-scientific support for the internal R&D, Marketing & Sales etc. departments Writing of Clinical Development Plans / Clinical Evaluation Plans and Reports, Post Market Clinical Follow Up Plans (and Reports) for new products and new indications
Your profile
Master of Science (MSc) degree in a natural science discipline or in the health sector, or equivalent qualification Doctorate (PhD or Dr.) is an advantage > 2 years of experience in planning and monitoring clinical trials Very good knowledge of the standard requirements ISO -GCP and 7/ for Medical Devices (MDR), as well as applicable FDA regulations Sound knowledge of clinical research/testing methodology Knowledge of the medical device industry and strong scientific understanding (experience in the field of medical devices, at least class II) Fluent in written and spoken English Any other language is an advantage
Your benefits
Working hours
Shiftwork, annual working hours, part-time
FlexWork
Work where and when you want (in Switzerland)
Up-to-date work environment
Up-to-date production, offices, break areas
Pension fund
Ypsomed covers % of the pension contributions
Mobility support
Charging stations, Swiss Half Fare Card, parking, close to public transport
Free sport facilities
Affordable or free gyms all over Switzerland
Family friendly
Financial contributions to childcare
Working hours
Shiftwork, annual working hours, part-time
FlexWork
Work where and when you want (in Switzerland)
Up-to-date work environment
Up-to-date production, offices, break areas
Pension fund
Ypsomed covers % of the pension contributions
Mobility support
Charging stations, Swiss Half Fare Card, parking, close to public transport
Free sport facilities
Affordable or free gyms all over Switzerland
Family friendly
Financial contributions to childcare
Working hours
Shiftwork, annual working hours, part-time
FlexWork
Work where and when you want (in Switzerland)
Up-to-date work environment
Up-to-date production, offices, break areas Your Ypsomed work environment { "name": "Ypsomed Company Movie EN", "description": "Ypsomed Company Movie EN", "thumbnailUrl": "uploadDate": "4--T::.+0", "contentUrl": "duration": "@context": "@type": "VideoObject" }
Ypsomed - making the treatment of chronic diseases possible
More than 2, employees worldwide develop and produce injection and infusion systems for self-medication with the Ypsomed Group. We are a successful, rapidly growing, family-owned company headquartered in Burgdorf (CH) with various production sites and subsidiaries around the world. With our market-leading products and solutions, we enable people all over the globe to self-treatment. Despite chronic diseases such as diabetes, obesity, or certain types of cancer, they are provided with the greatest possible quality of life.-
Clinical Research
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Solothurn, Schweiz TN Switzerland VollzeitSocial network you want to login/join with:Clinical Research & Evaluation Manager, SolothurnClient: YpsomedLocation: SolothurnJob Category: OtherJob Reference: 90956b1906f3Job Views: 10Posted: 21.01.2025Expiry Date: 07.03.2025Job Description:Responsible for overseeing global clinical trials, ensuring compliance with ISO, the Declaration of Helsinki, and...
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Scientific Services Manager.
Vor 3 Tagen
Solothurn, Schweiz Ypsomed VollzeitYour main tasks Perform medical assessments of technologies and therapies for the treatment of diabetes and translate into comprehensible insights to drive strategic decisions Develop, maintain and deliver medical and educational training programs to support the adoption of Ypsomed's solutions Create scientific materials to support the...