Remote Principal Medical Writer

Single sponsor Principal I/II Medical Writer (Clinical / Submissions exp) fully remote in Italy, UK, Spain, Poland or Ireland. Updated: Today Location: Remote, MI, Italy Job ID:25112590-OTHLOC-3531-2DR Description Single sponsor Principal I/II Medical Writer (Clinical / Submissions exp) fully remote in Italy, UK, Spain, Poland or Ireland. Syneos Health® is...

Overview As a Principal Medical Writer, you will lead high-quality scientific documents to support regulatory submissions and publications. You collaborate with clinical, regulatory, and medical affairs teams to translate data into clear narratives. The role is on-site in a collaborative environment that values expertise and innovation. You will shape...

Overview In this role you coordinate the operational management of assigned clinical projects to advance Chiesi’s pipeline in line with medical standards. You act as the primary liaison to CROs, providers, and internal stakeholders, ensuring study quality, timelines, and budget adherence. You play a key part in study design input and risk management,...

Il nostro cliente, realtà italiana in crescita, nata con l’obbiettivo di supportare le aziende nella digitalizzazione di tutti i processi presenti all’interno dei sistemi produttivi, ci ha incaricato di ricercare un/a: Il ruolo: La persona che stiamo cercando, rispondendo direttamente alla Direzione, avrà il compito di gestire, sviluppare e consolidare...

SALES ACCOUNT SPECIALIST BIOPROCESS La divisione Proper ricerca per conto di una realtà leader nella produzione e fornitura di soluzioni tecniche per il settore BioProcess, il Sales Account Specialist Bioprocess. La figura sarà responsabile dello sviluppo e della gestione commerciale del portafoglio clienti nel segmento BioProcess, con focus su soluzioni...

Overview In this role you coordinate the operational management of assigned clinical projects to advance Chiesi's pipeline in line with medical standards. You act as the primary liaison to CROs, providers, and internal stakeholders, ensuring study quality, timelines, and budget adherence. You play a key part in study design input and risk management,...

Overview In this role you coordinate the operational management of assigned clinical projects to advance Chiesi's pipeline in line with medical standards. You act as the primary liaison to CROs, providers, and internal stakeholders, ensuring study quality, timelines, and budget adherence. You play a key part in study design input and risk management,...

Overview In this role you coordinate the operational management of assigned clinical projects to advance Chiesi's pipeline in line with medical standards. You act as the primary liaison to CROs, providers, and internal stakeholders, ensuring study quality, timelines, and budget adherence. You play a key part in study design input and risk management,...

Overview As a Principal Medical Writer, you will lead high-quality scientific documents to support regulatory submissions and publications. You collaborate with clinical, regulatory, and medical affairs teams to translate data into clear narratives. The role is on-site in a collaborative environment that values expertise and innovation. You will shape...