14 opportunita di docs a Roma aggiornate oggi
offerte di lavoro trovate
A leading international law firm in Rome seeks a specialized Secretary to support a team of attorneys and partners. Responsibilities include managing agendas, making travel arrangements, drafting legal documents, and performing administrative tasks. Candidates must possess proven experience as a Leg
A leading international law firm in Rome seeks a specialized Secretary to support a team of attorneys and partners. Responsibilities include managing agendas, making travel arrangements, drafting legal documents, and performing administrative tasks. Candidates must possess proven experience as a Leg
Chiesi GroupA global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies. Candidat
FortreaA global pharmaceutical company is seeking a Senior Regulatory Medical Writer to lead the authoring and development of complex clinical regulatory documents. This role includes leading project teams, facilitating communication among stakeholders, and interpreting study data into concise documents. T
FortreaA global pharmaceutical company is seeking a Senior Regulatory Medical Writer to lead the authoring and development of complex clinical regulatory documents. This role includes leading project teams, facilitating communication among stakeholders, and interpreting study data into concise documents. T
Chiesi GroupA global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies. Cand
Chiesi GroupA global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies. Cand
Tubilux PharmaUn'azienda farmaceutica con sede a Pomezia cerca un Project Specialist per gestire progetti di ricerca e sviluppo. Il candidato ideale deve avere una Laurea in materie scientifiche e una comprovata esperienza nella gestione di progetti in aziende farmaceutiche. I requisiti includono una buona conosc
A global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies. Candidat
A global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. Si candidi in fretta: consulti la descrizione completa scorrendo verso il basso per scoprire tutti i requisiti di questo ruolo. This role requires leadership in managing cli
AltroA global pharmaceutical company is seeking a Senior Regulatory Medical Writer to lead the authoring and development of complex clinical regulatory documents. Tutti i potenziali candidati sono invitati a leggere con attenzione i seguenti dettagli prima di inviare la propria candidatura. This role inc
AltroA global pharmaceutical company is seeking a Senior Regulatory Medical Writer to lead the authoring and development of complex clinical regulatory documents. This role includes leading project teams, facilitating communication among stakeholders, and interpreting study data into concise documents. T
AltroA global pharmaceutical company is seeking a Senior Regulatory Medical Writer to lead the authoring and development of complex clinical regulatory documents. This role includes leading project teams, facilitating communication among stakeholders, and interpreting study data into concise documents. T
Chiesi GroupA global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies. Cand
18.000 € – 29.000 €/anno
Affidabilita della stima: Bassa
Stima basata sui dati di mercato per Roma. Gli stipendi effettivi possono variare in base a esperienza, azienda e zona.
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