...Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.We are an equal opportunities Recruitment Business and Agency. We w...
...Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.We are an equal opportunities Recruitment Business and Agency. We w...
...Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.We are an equal opportunities Recruitment Business and Agency. We w...
...Affairs, Quality Assurance, CMC, and the U.S. development partner.Manage documentation within the client’s electronic document management system (eDMS).Contribute to the preparation of regulatory subm...
...Affairs, Quality Assurance, CMC, and the U.S. development partner.Manage documentation within the client’s electronic document management system (eDMS).Contribute to the preparation of regulatory subm...
...Affairs, Quality Assurance, CMC, and the U.S. development partner.Manage documentation within the client’s electronic document management system (eDMS).Contribute to the preparation of regulatory subm...
...Affairs, Quality Assurance, CMC, and the U.S. development partner.Manage documentation within the client’s electronic document management system (eDMS).Contribute to the preparation of regulatory subm...
...Affairs, Quality Assurance, CMC, and the U.S. development partner.Manage documentation within the client’s electronic document management system (eDMS).Contribute to the preparation of regulatory subm...
...Affairs, Quality Assurance, CMC, and the U.S. development partner.Manage documentation within the client’s electronic document management system (eDMS).Contribute to the preparation of regulatory subm...
...Affairs, Quality Assurance, CMC, and the U.S. development partner.Manage documentation within the client’s electronic document management system (eDMS).Contribute to the preparation of regulatory subm...
...Affairs, Quality Assurance, CMC, and the U.S. development partner.Manage documentation within the client’s electronic document management system (eDMS).Contribute to the preparation of regulatory subm...
...Affairs, Quality Assurance, CMC, and the U.S. development partner.Manage documentation within the client’s electronic document management system (eDMS).Contribute to the preparation of regulatory subm...
Quality Manager (m/f/d) Early Clinical Trials Working hours: full-time Location: Biberach an der Riß Akkodis - formed through the merger of AKKA & Modis - is a global leader in engineering & IT. As a ...
...Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.We are an equal opportunities Recruitment Business and Agency. We w...
...Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.We are an equal opportunities Recruitment Business and Agency. We w...