science writer

472 offerte di lavoro science writer in Italia. Offerte aggiornate quotidianamente.


  • , Italia Etjca Group Tempo pieno

    Panoramica di PresentazioneL'azienda che sto supportando è un' Agenzia di Comunicazione Specializzata in Salute,Medical&Scientific Communication che opera nel Settore Heart Care .Job Title e finalità del RuoloSenior Medical WriterAll'interno di un contesto dinamico e in costante crescita, la risorsa avrà un ruolo strategico nella creazione, revisione e...


  • Roma, Provincia di Roma; Lazio, Italia Etjca Group Tempo pieno

    Panoramica di PresentazioneL'azienda che sto supportando è un' Agenzia di Comunicazione Specializzata in Salute,Medical&Scientific Communication che opera nel Settore Heart Care .Job Title e finalità del RuoloSenior Medical WriterAll'interno di un contesto dinamico e in costante crescita, la risorsa avrà un ruolo strategico nella creazione, revisione e...


  • Italia, Italia Etjca Group Tempo pieno

    L'azienda che sto supportando è un' Agenzia di Comunicazione Specializzata in Salute,Medical&Scientific Communication che opera nel Settore Heart Care . Senior Medical Writer All’interno di un contesto dinamico e in costante crescita, la risorsa avrà un ruolo strategico nella creazione, revisione e supervisione di contenuti medico-scientifici,...


  • roma, lazio, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • genova, liguria, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • treviso, veneto, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • reggio emilia, emilia romagna, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • catania, sicilia, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • trento, trentino alto adige, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • ancona, marche, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • pordenone, friuli venezia giulia, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • pisa, toscana, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • pavia, lombardia, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • prato, toscana, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • pescara, abruzzo, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • caserta, campania, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • salerno, campania, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • la spezia, liguria, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • belluno, veneto, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...


  • lecco, lombardia, Italia Biopharma Careers Tempo pieno

    Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet timelines.The role requires a life science degree, fluency in English, and strong experience...