Territory includes: Germany , Finland, Sweden and France
Qualified Candidates must be fluent in English
The Medical Affairs Company is initiating a global Field Medical team to support its client’s mission to redefine neuroscience drug deve...
For our Legal Partner department in Marburg, we are looking for a
Senior Project Manager - Legal Clinical Contracts (m/w/x) - R-224531
Fulltime / permanent / non-tariff (level 7)
The future position holder is accountable for the successful an...
Become part of our trainee club and start your career with a dual study program at ROSSMANN.
ROSSMANN has its own IT with more than 300 employees who work on exciting projects and solutions in three departments. Would you like to use your streng...
CRA I/II or Senior CRA Homebased across Germany
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
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...investigators and sites through the initial phase of a clinical study until the Site Initiation Visit.
The Local Start-up Specialist I/II is a member of the Study Start-up & Site Intelligence Unit.
Key Respons...
for full-time project work starting July 1, 2024 at the Infectious Disease and Tropical Medicine Department.
Our department at Heidelberg University Hospital has a clinical and research mandate. We are embedded in a research-active university ...
ICON 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 de...
...3rd semester in business, finance, environmental studies, engineering, or in a related field Cumulative 6 months of work experience (e.g. through previous internships) in start-ups, venture capital or climate tech ...
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Für Praktikanten
Praktikumsplatz
Traineeprogramm
Eschborn
Deutsche Gesellschaft für Internationale Zusammenarbeit
The Clinical Research Associate will perform site activities for Phase I-IV studies operating as the main point of contact for the site during a study. Drive and execute monitoring plans, ensure site GCP compliance, write trip reports, resolve issues...
