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19 Lavoro Regulatory Lead

UK/EU Regulatory Lead (IVD) BSI - it Great that you're thinking about a career with BSI!Job Title: Regulatory Lead(IVD)Reports to: Head of Notified Body IVDRLocation: EU / UK - homebasedOverview / Purpose of the position:Provide 5 giorni fa
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 4 giorni fa
Global Pharmaceutical Development Manager Adhr - Bolognana, LU responsibility (including process/product and analytical development) acting as the inter-face between development, management, operations, quality and regulatory functions. • Responsible for writing regulatory 17 giorni fa
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 6 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 10 giorni fa
Head Of Group Medical Regulatory EssilorLuxottica Group - Agordo, IT and lead the Regulatory Status at Global level for Medical Devices topics and with a specific focus on MDR. • Oversee the implementation and maintenance of policies and procedures related to quality Più di 30 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 11 giorni fa
Senior Clinical Data Manager - single sponsor Fortrea - 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 10 giorni fa
Director, Regulatory Operations Association-American Cancer Institute - 50121 Firenze , training, SOP management, user group engagement, trial migration, and quality control.Identify Consortium and Central Regulatory improvement opportunities and lead improvement efforts within team, including Più di 30 giorni fa
Senior Statistical SAS Programmer, Oncology, Single Sponsor - Home Based or Office Based Fortrea - 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 10 giorni fa

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