Study Start-up Specialist
vor 3 Wochen
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 leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time office-based Regulatory Submissions Coordinator/Study Start-up Specialist 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 expertise and can develop and grow your career even further, then this is the opportunity for you. Entry-level positions with permanent contract are available for recent graduates. Responsibilities Prepare, review, and file clinical trial applications for Germany, Austria and Switzerland (DACH); Communicate with research sites in Germany, Austria and Switzerland (hospitals, etc.) to collect all essential documents required before the site starts to enroll patients to participate in the clinical trial; Provide insightful input on regulatory submissions documents and maintain timelines for study start-up through both internal and external collaboration; Ensure submissions comply with applicable regulations and guidance documents; Advise on changing country regulations and compliance requirements; and Track submissions and ensure timely filing of documents. Qualifications Bachelor's degree (preferably in a Life Sciences field); Interest in drug development and clinical trials; Full professional proficiency in German and English in written and verbal communication; Knowledge of Microsoft® Office; and Excellent organization and communication skills, great attention to detail. Travel: None We kindly ask to submit applications in English. We would appreciate if you could indicate the status of your work permit if needed.
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Study Start Up Site Navigator based in Germany
vor 1 Woche
München, Deutschland Fortrea Vollzeit 35.000 € - 55.000 € pro JahrJoin Fortrea's mission to transform clinical trials and improve patient outcomes.As a Study Start Up Site Navigator in Germany, you'll support site activation activities and help ensure smooth collaboration between study teams and clinical sites. This is an excellent opportunity to start your career in clinical research within a dynamic, global...
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Study Start Up Lead with Finance expertise
vor 4 Wochen
München, Deutschland Fortrea VollzeitWe are looking for a sponsor-dedicated Country Start-Up Lead to oversee clinical trial site activation, regulatory processes, and financial management . This is a well suited role for someone with experience in clinical start-up operations, budget negotiations, and regulatory compliance and who enjoys working collaboratively to drive progress. Key...
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München, Deutschland Fortrea Vollzeit 60.000 € - 120.000 € pro JahrJoin Our Team and Drive Clinical Research SuccessAt Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist, you will play a pivotal role in coordinating site start-up activities, managing essential documents, and ensuring regulatory submissions are completed efficiently. Your expertise will...
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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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Mgr Medical Study Operations
vor 1 Woche
München, Deutschland Regeneron VollzeitAt Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to approach science, manufacturing and commercialization. And new ways to think about...
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Experienced Regulatory Submissions
vor 2 Wochen
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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Senior Communication Specialist
vor 2 Wochen
München, Deutschland Pixida Group VollzeitTasks \ > As a Senior Communication Specialist at Pixida Group, you will play a pivotal role in shaping our marketing and brand strategies across diverse markets and support business growth. \ > You will collaborate effectively with cross-functional teams to develop and execute communication strategies that support corporate objectives. \ > Create...
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Clinical Trial Coordinator
Vor 3 Tagen
München, Deutschland Alira Health VollzeitJoin our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description...
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Recruiting Specialist
vor 1 Woche
80687 München, Deutschland bravobike GmbH Vollzeit**Lust auf eine besondere Herausforderung in einem sehr people-orientierten Scale-up?** Bei uns dreht sich alles um die Menschen, den Sinn und den Erfolg. Wir möchten Großes erreichen und du wirst dabei eine entscheidende Rolle spielen. Wir suchen aktuell nach Verstärkung in unserem People-Team, um unser Wachstum weiter voranzutreiben. Als Recruiting...
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Supply Chain Specialist
vor 1 Woche
München, Deutschland bravobike GmbH VollzeitLust auf eine besondere Herausforderung? Teilst du unsere Vision von einer nachhaltigen und fairen Mobilitätszukunft und hast eine Leidenschaft für Supply-Chain-Prozesse sowie ein Gespür für effiziente Lieferketten? Dann werde als Supply Chain Specialist (d/w/m) ein wichtiger Teil unserer Fahrradwelt und sorge für eine reibungslose Bereitstellung von...