21.05.24 | Vollzeit | Freising | Daiichi Sankyo Europe GmbHReview and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy, expectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management
Später ansehen21.05.24 | Vollzeit | Augsburg | Formycon AGDevelopment. In this role you will lead a team of ≥ 5 RA managers. You will be acting as a regulatory expert coaching your team and aligning regulatory strategies with experts from various departments, external partners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management
Später ansehen21.05.24 | Vollzeit | München | Daiichi Sankyo Europe GmbHReview and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy, expectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management
Später ansehen21.05.24 | Vollzeit | Landsberg am Lech | Daiichi Sankyo Europe GmbHReview and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy, expectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management
Später ansehen21.05.24 | Vollzeit | München | Daiichi Sankyo Europe GmbHReview and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy, expectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management
Später ansehen21.05.24 | Vollzeit | Augsburg | Formycon AGDevelopment. In this role you will lead a team of ≥ 5 RA managers. You will be acting as a regulatory expert coaching your team and aligning regulatory strategies with experts from various departments, external partners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management
Später ansehen21.05.24 | Vollzeit | Augsburg | Formycon AGDevelopment. In this role you will lead a team of ≥ 5 RA managers. You will be acting as a regulatory expert coaching your team and aligning regulatory strategies with experts from various departments, external partners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management
Später ansehen21.05.24 | Vollzeit | Augsburg | Formycon AGDevelopment. In this role you will lead a team of ≥ 5 RA managers. You will be acting as a regulatory expert coaching your team and aligning regulatory strategies with experts from various departments, external partners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management
Später ansehen21.05.24 | Vollzeit | Augsburg | Formycon AGDevelopment. In this role you will lead a team of ≥ 5 RA managers. You will be acting as a regulatory expert coaching your team and aligning regulatory strategies with experts from various departments, external partners and CDMOs. Your reporting line is to the VP Regulatory Affairs and Quality Management
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