28.05.24 | Vollzeit | Tübingen | Immatics Biotechnologies GmbHProject team Contribution to preparing clinical trial associated documents with a focus on immunological and Immunomonitoring associated aspects (e.g., Clinical Study Protocol, Clinical Study Report, Statistical Analysis Plan etc.) Support of Quality Management including writing and reviewing of Standard
Später ansehen28.05.24 | Vollzeit | Sindelfingen | Immatics Biotechnologies GmbHProject team Contribution to preparing clinical trial associated documents with a focus on immunological and Immunomonitoring associated aspects (e.g., Clinical Study Protocol, Clinical Study Report, Statistical Analysis Plan etc.) Support of Quality Management including writing and reviewing of Standard
Später ansehen28.05.24 | Vollzeit | Stuttgart | Immatics Biotechnologies GmbHProject team Contribution to preparing clinical trial associated documents with a focus on immunological and Immunomonitoring associated aspects (e.g., Clinical Study Protocol, Clinical Study Report, Statistical Analysis Plan etc.) Support of Quality Management including writing and reviewing of Standard
Später ansehen28.05.24 | Vollzeit | Böblingen | Immatics Biotechnologies GmbHProject team Contribution to preparing clinical trial associated documents with a focus on immunological and Immunomonitoring associated aspects (e.g., Clinical Study Protocol, Clinical Study Report, Statistical Analysis Plan etc.) Support of Quality Management including writing and reviewing of Standard
Später ansehen28.05.24 | Vollzeit | Leonberg | Immatics Biotechnologies GmbHProject team Contribution to preparing clinical trial associated documents with a focus on immunological and Immunomonitoring associated aspects (e.g., Clinical Study Protocol, Clinical Study Report, Statistical Analysis Plan etc.) Support of Quality Management including writing and reviewing of Standard
Später ansehen28.05.24 | Vollzeit | Rottenburg am Neckar | Immatics Biotechnologies GmbHProject team Contribution to preparing clinical trial associated documents with a focus on immunological and Immunomonitoring associated aspects (e.g., Clinical Study Protocol, Clinical Study Report, Statistical Analysis Plan etc.) Support of Quality Management including writing and reviewing of Standard
Später ansehen28.05.24 | Vollzeit | Sindelfingen | Immatics Biotechnologies GmbHProject team Contribution to preparing clinical trial associated documents with a focus on immunological and Immunomonitoring associated aspects (e.g., Clinical Study Protocol, Clinical Study Report, Statistical Analysis Plan etc.) Support of Quality Management including writing and reviewing of Standard
Später ansehen28.05.24 | Vollzeit | Reutlingen | Immatics Biotechnologies GmbHProject team Contribution to preparing clinical trial associated documents with a focus on immunological and Immunomonitoring associated aspects (e.g., Clinical Study Protocol, Clinical Study Report, Statistical Analysis Plan etc.) Support of Quality Management including writing and reviewing of Standard
Später ansehen28.05.24 | Vollzeit | Filderstadt | Immatics Biotechnologies GmbHProject team Contribution to preparing clinical trial associated documents with a focus on immunological and Immunomonitoring associated aspects (e.g., Clinical Study Protocol, Clinical Study Report, Statistical Analysis Plan etc.) Support of Quality Management including writing and reviewing of Standard
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