Locations: Berlin, Germany Categories: Clinical Research Associate Req ID: 12973 For Clinical Study Coordinators located in Berlin: The Clinical Research Associate role at Medpace is offering the unique opportunity to have an exciting career in the research
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical
JOB DESCRIPTION Job title: Compliance Officer Wholesale and Regulatory Compliance Corporate Title: Vice President / Executive Director Contract Duration: 12 Months Fixed Term Contract Department: Wholesale Compliance Location: Frankfurt am Main, Germany The base pay range for
Study Start Up Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
Job Description: In order to support the Spectrum & Regulatory Affairs team, Airbus Defence and Space is looking for a Working Student within Frequency Management (d/f/m) You are a full time student, looking for a working student
The Position The Study Physician role is a critical position within Clinical Development Inflammation, providing readily available, high-quality medical support and consultancy for global clinical trials. As a qualified and clinically experienced physician, you will contribute to
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Regulatory Affairs Manager As a Regulatory Affairs Manager, youll offer innovative solutions, including regulatory affairs expertise and client interface, to provide strategic regulatory intelligence and guidance supporting product development
Senior Study Start Up Associate At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development
Job Title: Regulatory and Start-Up Specialist 1 Location: Frankfurth, Germany Job Overview: The Regulatory and Start-Up Specialist 1 is responsible for supporting the site identification process and performing regulatory start-up and maintenance activities in accordance with regulations SOPs and
Mission Neko is redefining what prevention means, from treating illness when it arrives, to sustaining health before its ever at risk. Our mission: make data-driven, preventative care accessible to more people, before symptoms appear. In a
In AstraZenecas Cell Therapy division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying, and even curing some of the worlds most complex diseases. We have the potential to grow
This is what you will do: The Medical Excellence- and Project Manager is part of the Medical Affairs & Medical Operations team. This role is responsible for ensuring that strategy, processes, competencies, tools and quality standards
Sr. Site Contracts Associate IQVIA Biotech Germany - Homebased IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic
Since 1961, NERA (https://www.nera.com) has provided unparalleled guidance on the most important market, legal, and regulatory questions of the day. Our work has shaped industries and policy around the world. Our field-leading experts and deep experience allow
Company:NERA Description: Since 1961, NERA (https://www.nera.com) has provided unparalleled guidance on the most important market, legal, and regulatory questions of the day. Our work has shaped industries and policy around the world. Our field-leading experts and deep
Job Description At Boeing, we innovate and collaborate to make the world a better place. We’re committed to fostering an environment for every teammate that’s welcoming, respectful and inclusive, with great opportunity for professional growth. Find
The Principal Biostatistician will serve as the statistical lead for clinical studies, providing scientific oversight, strategic guidance, and hands‑on statistical support across late‑phase clinical trials. This role requires a highly experienced biostatistician capable of working independently, representing
The Site Contracts Associate (SCA) is responsible for ensuring that site contracts follow all relevant legal rules, internal guidelines and agreed negotiation parameters with clients. The Site Contracts Associate will review and amend contracts (specifically Clinical
The Company kp is a globally recognised leader in the packaging and specialty film industry, renowned for its unwavering commitment to sustainability and innovation. The need to act on climate change has never been clearer so
We’re flexible! We’re happy to receive applications in English or German. Your tasks: In your role, you will support the ICT Security Change Services (SCS) team in day-to-day operations and strategic initiatives by contributing to the