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... Development, Manufacturing Sciences and Technologies, Regulatory Affairs, and other Cell Therapy Development ... Therapy Development Organizations to ensure regulatory compliance of GMP operations in ... manufacturing sciences and technology,..
This position is eligible for the Education Debt Reduction Program (EDRP), a student loan payment reimbursement program. You must meet specific individual eligibility requirements in accordance with VHA policy and submit ..
... The S&E team interacts with biotech and biopharma companies, academic institutions, ... attractive opportunity for an experienced biotech or pharmaceutical industry professional who ... experience in the pharmaceutical or..
... diseases. SummaryThe Senior Associate supports Regulatory leadership in the development and ... of global nonclinical / clinical regulatory strategies through a programu2019s lifecycle.u00A0 ... for HA interactions and complete..
... lives. SummaryThe Senior Manager supports Regulatory leadership in the development and ... of global nonclinical / clinical regulatory strategies through a programu2019s lifecycle.u00A0 ... interactions and the oversight of..
Who We Are For more than two decades, going our own way has led to countless breakthroughs, bettering the lives of those suffering from rare genetic disease. In 1997 we were ..
... to support nonclinical reports and regulatory submissions.rnrnThe Operations Specialist, Nonclinical Development ... will also work closely with Regulatory Affairs to prepare, format, and publish ... and publish documents to..
... DESCRIPTIONAs a Senior/Executive Director in Regulatory Affairs, CMC, focusing on diagnostics and ... responsible for establishing the overall regulatory strategy for contemporaneous development of ... will serve to develop..
... preparation, and submission of CMC regulatory documentationThis includes supporting the global ... CMC strategy for the Global Regulatory Plan, with input from regional ... Plan, with input from regional..
... lives. Responsibilities Analyst role for Regulatory Research & Intelligence (RRI) includes: ... Intelligence (RRI) includes: Supporting senior regulatory research staff involved in examining ... research staff involved in examining..
... to help patients. OverviewBioMarin Global Regulatory Affairs (GRA)u00A0is responsible for obtaining approval ... as the interface between the regulatory authorities and the program teams ... plan correctly anticipates what..
... Clinical Development, Clinical Science, Research, Regulatory Affairs, Biometrics, and Quality Assurance. The ... and documentation for submission to regulatory agencies (IND, BLA). Develop and ... counterparts in Early Development,..
Job Summary: The Regulatory Operations Sr. Manager, Publishing will ... for the preparation of global regulatory submissions. This position will collaborate ... position will collaborate closely with Regulatory Affairs and..
... development activities including preparation of regulatory submissions for the target clinical ... CRO management, clinical support of regulatory interaction, and study analysis and ... and reporting). Partner with Research,..
... and execution, data analysis and regulatory filings as delegated by the ... components of trial execution and regulatory submission (including IND Annual Reports, ... treatment, drug development trends, and..
The Northern Arizona VA Health Care System (NAVAHCS) is currently recruiting for a Medical Technologist (Technical Specialist) to work in the Pathology and Laboratory Medicine Service, Prescott, Arizona. Applicants pending the ..
... role supporting BioMarinu2019s Global Medical Affairs function within the Worldwide Research ... partner for the Global Medical Affairs organization.u00A0 Collaborate with business partners ... skillsDesired Skills:u00A0 u00A0 u00A0 u00A0..