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...
...Workflow Manager Cranial Tumor (m/w/x) page is loaded Workflow Manager Cranial Tumor (m/w/x)
Apply locations Oberkochen time type Full time posted on Posted 2 Days Ago job requisition id JR_1026413 Your Role:
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Research Data Manager / Data Steward (f/m/x)
Institute of Biomedical Informatics pan
as soon as possible
full-time; initially limited for 2 years according to WissZeitVG Drittmittel with the option to extend
Your salary will be based on...
...takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank yo...
...Higher Education Act (BerlHG). Procedures, processes and performance criteria are set out in the Charité – Universitätsmedizin Berlin’s statute governing tenure-track professorships .
The professorship can also...
Manager* IMP Manufacturing
Manager* IMP Manufacturing QA
This position is limited to one year.
As Manager* IMP Manufacturing QA you will be acting as QA representative for specific clinical trial programs within our ...
Coronary Vascular Intervention Clinical Specialist: Chicago
As one of the world´s leading manufacturers of cardio- and endovascular medical devices, BIOTRONIK is headquartered in Berlin, Germany, and represented in over 100 countries by its...
...party funding with the option of extension remuneration according to TV-L
" Your tasks
The Institute for Biomedical Informatics (BI-K) & the Medical Data Integration Center (MeDIC) at the University Hospital of...
Fresenius Medical Care is the world's leading provider of products and services for individuals with renal diseases. As a global health care company, we have
a special goal: provide the best possible care. Join us to improve the quality of life for...
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...
