10.06.24 | Vollzeit | Ottobrunn | JobLeads GmbH | 150.000 € - 200.000 € Equal opportunities for all. As such, we will never ask for any type of monetary exchange in the frame of a recruitment process. Any impersonation of Airbus to do so should be reported to emsom@ . At Airbus, we support you to work, connect and collaborate more easily and flexibly. Wherever
Später ansehen21.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Freising | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Landsberg am Lech | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Freising | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Germering | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
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