Lavoro Clinical Regulatory Lead
CMC Services Regulatory Affairs Specialist
Thermo Fisher Scientific - Monza, Lombardy, it
. Write and review of CTD Module 3.2.P Drug Product for new Marketing Authorizations, variations and renewals and for Clinical Trials Applications (CTAs). Support Clients in answering to Regulatory
da: it.talent.com - 12 giorni fa
Regulatory Affairs Professional - CTA/EU-CTR (1 year FTC)
Parexel - it
Submission Coordinator/Lead, overseeing complex large clinical trial submissions.Role Responsibilities:Provide leadership and expertise in regulatory and submissions related aspects of clinical trialsAct as
da: it.talent.com - 8 giorni fa
Adhr - Bolognana, LU
packages for clinical/marketing authorizations with very limited supervision. • Lead with limited supervision assigned projects and/or complex sub-projects according to product portfolio needs. Requirements
da: performahrm.com - 14 giorni fa
Senior Clinical Data Manager - FSP (oncology experience)
Fortrea - Rome, Lazio, it (+2 località)
to support operations.Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.Ability to lead teams by example on project
da: it.talent.com - 7 giorni fa
Senior Statistical SAS Programmer, Oncology, Single Sponsor - Home Based or Office Based
Fortrea - Milan, Lombardy, it (+1 località)
central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies
da: it.talent.com - 7 giorni fa
Director, Regulatory Operations
Association-American Cancer Institute - 50121 Firenze
effective integration between regulatory and clinical operations.Oversee management and system support for an enterprise-wide eRegulatory and eSubject management system, Florence, including on-boarding
da: it.jobtome.com - Più di 30 giorni fa
Pharmaceutical Development Manager
Kedrion Biopharma - Bolognana, Tuscany, it
development, management, operations, quality and regulatory functions.• Responsible for writing regulatory packages for clinical/marketing authorizations with very limited supervision.• Lead with limited
da: it.talent.com - 7 giorni fa
Senior Clinical Data Manager - single sponsor
Fortrea - Milan, Lombardy, it (+2 località)
support operations.Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.Ability to lead teams by example on project strategies
da: it.talent.com - 7 giorni fa
Solution Architect - Veeva Vault - Life Sciences
NNIT - it (+1 località)
Veeva Vault (Quality, Regulatory or Clinical) systems. Provide subject matter expertise on the Veeva Vault (Quality, Regulatory or Clinical), technical design, and implementation best practices. Execute
da: it.talent.com - 11 giorni fa
CMC Services Regulatory Affairs Specialist
Thermo Fisher Scientific - Monza, Lombardy, it
Drug Product for new Marketing Authorizations, variations and renewals and for Clinical Trials Applications (CTAs).Support Clients in answering to Regulatory Authorities Deficiency Letters.In additon
da: it.talent.com - 12 giorni fa