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. the names and contact information for two referees. One of these should be the main advisor for the master's thesis or equivalent thesis CV transcripts and diplomas showing completion of the bachelor's and
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institution systems may be submitted. Click here for detailed information about acceptable transcripts. A current resume/CV, including academic history, employment history, relevant experiences, and
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) a research PhD alongside their medical degree or equivalent clinical professional qualification. Application deadline: 30 April 2026 For information on how to apply, please click on the 'Apply' button
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. The Research Fellow will undertake high-quality research both independently and collaboratively, producing scholarly outputs and engaging with policy actors, UN agencies and other stakeholders to support data
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industry, government, and professional bodies. This is a research focused position. Further information can be found by viewing UQ’s Criteria for Academic Performance . About the Food and Beverage
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single parents with children accompanying them allowance for research costs to be paid to the hosts extensive alumni sponsorship Application Papers All application forms and further information
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powered by: Cookie Information Nettsiden bruker cookies Vi ønsker at du skal være trygg når du bruker dette nettstedet. Vi benytter cookies for å sikre at du får en best mulig brukeropplevelse og
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within the Institute. This role is suitable for individuals who hold, or will have been awarded by the start date, a PhD/DPhil in AI Ethics and/or Data Ethics and/or Neuroethics and/or Philosophy
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Max Planck Institute for Comparative Public Law and International Law, Heidelberg | Heidelberg, Baden W rttemberg | Germany | 9 days ago
academic referees Contact information For inquiries about the group or the position, please contact Dr Carolyn Moser or her assistant Rocío Bargon Sánchez at ensure@mpil.de .
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Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | 3 days ago
methodology, and translational research design. The participant will develop competencies in good clinical practice (GCP) standards, clinical trial ethics, protocol development, pharmacokinetic data analysis