21.05.24 | 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 | 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 | Augsburg | Formycon AGPartners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management. Your main tasks include the following Align RA CMC DP strategy for Formycon’s development projects and approved products (focus on aseptically manufactured parenteral products in various dosage forms
Später ansehen21.05.24 | Vollzeit | Fürstenfeldbruck | 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 | Erding | 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 | Augsburg | Formycon AGPartners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management. Your main tasks include the following Align RA CMC DP strategy for Formycon’s development projects and approved products (focus on aseptically manufactured parenteral products in various dosage forms
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 | München | 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
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