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Clinical Regulatory Affairs Online Resumes
Clinical Regulatory Affairs
Clinical Regulatory Affairs
Clinical Regulatory Affairs
Mexico
Able to expedite the documents required by Latin America BoH. Knowledge of the different sections (CTD) that have direct impact on the product. Knowledge of Latin America regulations relative to pharmaceutical and nutritional products. Capable of preparing documents for registration, variations and product renewals.. Knowledge of Good Documentation Practices. Able to expedite legal documents that make up a dossier. Evaluati...
Clinical Regulatory Affairs
Clinical Regulatory Affairs
Clinical Regulatory Affairs - 3 Years of Experience - Near 02120
Clinical Regulatory Affairs
Professional Summary Regulatory affairs associate adept in research and documentation of product dossier. Provide clear and concise information based on creative and complex findings. Also a dedicated lecturer with a stong work ethic. Skillfully manages lectures and promotes open classroom discussions. Regulatory affairs associate Jan 2011 - Feb 2012 Alice Pharma Pvt Ltd Mumbai, India * Regulatory Dossiers Preparation. * Co...
Tags for this Online Resume: Business Development, Communication Skills, Documentation, Excellent Communication Skills, Laboratory Work, Management, Market Research, Microsoft
Clinical Regulatory Affairs
Ideal Companies: Pharma/Biotech Co., Research Org.
Tags for this Online Resume: Health Care Industry, Integrate, Managed Care, Pharmaceutical, Protocol, Quality Assurance, Sales, Test, Business Analysis, Business Development
Regulatory Affairs - 15 Years of Experience - Near 94565
Regulatory Affairs professional seeking to change industries for petrochemical regulatory matters to biotech and medical device industry. Proven aptitude to in dealing with regulatory authorites with special expertise in the Asia Pacific region.
Clinical Regulatory Affairs - 5 Years of Experience - Near 58102
Tags for this Online Resume: Medicare, Healthcare, SharePoint, PECOS, MS Office, MS Access, Me Excel
Clinical Regulatory Affairs - 13 Years of Experience - Near 19711
My background includes six years experience as a Project Manager for Regulatory Global submissions, as well as Life Cycle Management of Regulatory documents. As a Project Manager within the Submission Management Group, I provided expertise on global submission compilation and published electronic submissions compiled in RSS Application (eCTD) in accordance with Health Authority guidelines and departmental standards.
Tags for this Online Resume: Newark, DE, eCTD, RSS Application, Regulatory Publisher, Regulatory Submissions, Document Management, Legal, Management, Project Management, Publishing, Quality Assurance, Test, eCTDXpress
