We are looking for an experienced Regulatory/Medical Writer who is ready to step into a more consultative, client-facing role. While you’ll bring deep hands-on expertise in regulatory document authorship, this position is focused less on day-to-day...
studies in Phases I-IV and across studies for submission in various therapeutic areas, including both medical device and drug settings.
KEY RESPONSIBILITIES
• Carry out tasks within the specified timelines and quality standards.
• Supervise tasks carried...
garantire la pianificazione e l’organizzazione di Advisory Boards;
• garantire la revisione medica continua di pubblicazioni scientifiche e la valutazione della loro rilevanza per la strategia locale dell’Azienda;
• condurre presentazioni scientifiche (PDP)...
clinical studies, raise manual queries for uncoded terms as required.
• Query management: review discrepancies, review answered queries, resolve and close where appropriate, manage the data cleaning process including manual checks and Medical Review...
like scientific publications and advisory boards
• Identify and develop peer-to-peer relationships with country KOLs, as well as other influencers and leaders of the scientific and healthcare community, utilizing scientific and medical evidence-based...
We are looking for an experienced Regulatory/Medical Writer who is ready to step into a more consultative, client-facing role. While you’ll bring deep hands-on expertise in regulatory document authorship, this position is focused less on day-to-day...