Regulatory Officer
vor 3 Wochen
Company Description PSI is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Regulatory Officer Munich, Germany I Full-time Job Description Join our team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating the start of research projects of novel medicinal products, while taking a step further in your professional career. Office-based in Munich/Planegg Your role: Prepare clinical trial submission dossiers for Regulatory and Ethics Authorities, including Import and Export license applications Communicate with regulatory authorities, ethics committees, project teams and vendors on regulatory-related matters Review translations of essential documents subject to clinical trial submission Track the regulatory project documentation flow Review documents to greenlight IP release to sites Manage safety reporting to authorities Deliver regulatory training to project teams Assist with feasibility research and business development requests Qualifications College/University degree or an equivalent combination of education, training and experience Prior experience with clinical trial submissions in Germany Full working proficiency in English and German Proficiency in MS Office applications Detail-oriented Ability to learn, plan and work in a dynamic team environment Communication, collaboration, and problem-solving skills Additional Information We offer: Excellent and flexible working conditions Extensive training and friendly, collegial team Competitive salary and benefits package Opportunities for personal and professional growth If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. I'm interested
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Regulatory Officer
vor 3 Wochen
München, Deutschland PSI CRO Deutschland GmbH VollzeitCompany DescriptionPSI is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Regulatory Officer Munich, Germany I Full-time Job DescriptionJoin...
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Regulatory Officer
vor 4 Wochen
München, Deutschland PSI CRO Deutschland GmbH VollzeitCompany Description PSI is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Regulatory OfficerMunich, Germany I Full-time Job Description Join...
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Regulatory Affairs Manager
Vor 5 Tagen
München, Deutschland Cpl Life Sciences Vollzeitob Title: European Regulatory Affairs Manager Location: Munich, Germany - Hybrid, 3x a week in the office Remuneration: Competitive salary and package Regulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is increasingly growing and is looking for a...
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Specialist, Regulatory
vor 4 Wochen
München, Deutschland Medpace VollzeitMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. Our clinical operations...
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Compliance Regulatory Liaison, Vice President
Vor 3 Tagen
München, Deutschland State Street VollzeitWho we are looking for: SSBI (State Street Bank International) Compliance Regulatory Liaison reports directly to SSBI Head of Compliance, and collaborates closely with SSBI Senior Management and State Street Global Compliance Regulatory Liaison Office. In this role you will contribute to fostering a positive regulatory culture and promoting proactive...
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Senior Manager/Director of Regulatory Affairs
Vor 5 Tagen
München, Deutschland Cpl Life Sciences Vollzeitob Title: European Regulatory Affairs Manager Location: Munich, Germany - Hybrid, 3x a week in the office Remuneration: Competitive salary and package Regulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is increasingly growing and is...
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Experienced Regulatory Submissions
vor 1 Woche
München, Deutschland Medpace VollzeitMedpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We...
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Regulatory Submissions Coordinator
vor 2 Wochen
München, Deutschland Medpace, Inc. VollzeitJob Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a full-time** office-based** Regulatory Submissions Coordinator to join our Clinical Operations team in **Munich**. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous...
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Senior) Regulatory Affairs Expert
vor 18 Stunden
München, Deutschland Ebenbuild Vollzeit**Your mission**: We want you to join our early-stage university spin-off that has just received its ISO 13485 certification. As an integral part of our team, you will harness your regulatory expertise to - develop and implement the regulatory strategy for FDA clearance (De Novo) and conformity assessment under MDR (class II). - create, manage, and maintain...
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Regulatory Affairs Coordinator
Vor 2 Tagen
München, Deutschland Constares GmbH VollzeitUnser Kunde ist ein führendes biopharmazeutisches Unternehmen mit Sitz in München. Ihr Aufgabenbereich: Pflege der öffentlich zugänglichen und internen webbasierten Regulatory-Seiten, Zusammenstellung von Berichten/Übersichten, Erstellung von Präsentationen Unterstützung bei Textprüfungen/Korrekturlesen (Packungsbeilagen, Verpackungsmaterial,...