Jobs für clinical data manager bei Hessen

Your ResponsibilitiesPlanning, organization, execution, oversight and evaluation of national and international clinical trials (Phase I-IV, focus on nutrition clinical studies) according to ICH-GCP, other applicable legislations and internal standard operating procedures (SOPs). This includes the following tasks:Management of clinical studies according to...

Clinical trial manager, CTM, germany, sponsor dedicatedICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Clinical Trial...

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client's project team in the execution of early clinical trials. Joining our team offers the opportunity to work on innovative projects in a dynamic environment. You will support trial preparation, documentation, and coordination, ensuring...

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client's project team in the execution of early clinical trials. Joining our team offers the opportunity to work on innovative projects in a dynamic environment. You will support trial preparation, documentation, and coordination, ensuring...

IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client's project team to set-up and execute clinical trials. Joining the sponsor-dedicated team provides the opportunity to work with early phase clinical research projects (phase I and II) in different therapeutic areas.As Clinical Trial...

Klinische Forschung unter besseren Bedingungen - Wir vereinen akademisches Wissen und medizinisches Können mit wirtschaftlicher Flexibilität.Die GBG Forschungs GmbH ist ein unabhängiges und akademisches Forschungsinstitut (ARO), welches klinische Studienprojekte zur Verbesserung der Therapiemöglichkeiten von Brustkrebs entwickelt, durchführt und...

EPM Scientific are currently partnered with a client running a global project in Aesthetic Medicine. They are urgently seeking a Freelance Clinical Research Associate to support their expanding clinical operations team. See a short summary below:Contract Conditions:Start date: FebruaryLocation: Germany, RemoteContract Type: Freelance / Consultant FTE, 12...

CRA II, Clinical Research Associate, Senior CRAICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Senior Clinical Research...

Clinical Research Associate - French / German Speaking - Remote - FSPICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a...

Die Rolle Als Senior Clinical Project Manager steuern Sie klinische Studien mit Fokus auf wissenschaftliche Integrität, methodische Präzision und effiziente Umsetzung. Sie koordinieren interdisziplinäre Teams, erkennen Risiken und betreuen Studien valide, reproduzierbar und regulatorisch belastbar. Die Mission Wissenschaftliche Qualität,...

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client's project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas in Germany or the DACH region. You...

Clinical Trial Educators (CTEs) collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance. They lead relationship management and communication of medical and...

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client's project team in the execution of clinical trials. Joining the team provides the opportunity to work with one single client and to manage clinical research projects in different therapeutic areas.We currently offer the exciting opportunity...

Join IQVIA as aClinical Research Associate 1orClinical Research Associate2/ CRA I or CRA IIand workhome-based throughout Germanyin oursingle sponsor department.You will enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients.Whether you're just starting out or looking to...

Make an impact with NTT DATA Join a company that is pushing the boundaries of what is possible. We are renowned for our technical excellence and leading innovations, and for making a difference to our clients and society. Our workplace embraces diversity and inclusion – it's a place where you can grow, belong and thrive. Senior Manager Field Support...

Local Trial Manager - FSP - RemoteICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Clinical Trial Manager to join our...

Make an impact at NTT Global Data CentersJoin NTT Global Data Centers and be part of a team that drives innovation and sustainability in the digital world. With over 150 data centers across more than 20 countries globally, we offer unparalleled opportunities to work on cutting-edge technology and transformative projects. Experience a collaborative,...

Key ResponsibilitiesCoordinate centralized support for uploading CPP documents (e.g., population PK/PD data transfer plans, analysis plans, and reports) into regulatory systems in compliance with global procedures.Prepare and review CPP documents for submission, ensuring accuracy, consistency, and inspection readiness.Provide scientific writing support for...

Job Overview We are seeking an experienced Regulatory Affairs Manager to join our Global Regulatory Affairs team, supporting the development of small molecule drug products across clinical development phases I–III. This role will play a key part in shaping and executing global regulatory strategies to enable efficient clinical development and timely...

About Vantage Data CentersVantage Data Centers powers, cools, protects and connects the technology of the world's well-known hyperscalers, cloud providers and large enterprises. Developing and operating across North America, EMEA and Asia Pacific, Vantage has evolved data center design in innovative ways to deliver dramatic gains in reliability, efficiency...