9 Lavoro Clinical Regulatory Lead
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Senior Statistical SAS Programmer, Oncology, Single Sponsor - Home Based or Office Based Fortrea - Milan, Lombardy, it 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 5 giorni fa
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Senior Clinical Data Manager - single sponsor Fortrea - Milan, Lombardy, it 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 5 giorni fa
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Global Pharmaceutical Development Manager 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 24 giorni fa
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Senior Clinical Data Manager - FSP (oncology experience) Fortrea - it 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 5 giorni fa
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Principal Medical Writer, sponsor-dedicated, EMEA Fortrea - it can´t do it alone. We are seeking an experienced Medical Writer to lead authoring and development of high complexity clinical regulatory documents that are critical to the project(s) and strategic goals 11 giorni fa
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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 Più di 30 giorni fa
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Associate Director, Clinical Portfolio Execution CSL - Siena, Tuscany, it associated documents.Responsible for leading vendor selection and management/ oversight, including issue escalation.Lead a cross functional team ensuring timely EC/ IRB and regulatory submissions.Ensure 13 giorni fa
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Regulatory Affairs Consultant - CTA/EU-CTR (1 year FTC) Parexel - it Coordinator/Lead, overseeing complex large clinical trial submissions.Role Responsibilities:Provide leadership and expertise in regulatory and submissions related aspects of clinical trialsAct as the main 14 giorni fa
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Senior Clinical Data Manager - FSP (oncology experience) Fortrea - Milan, Lombardy, it 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 14 giorni fa
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