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Online Resumes with "Clinical Regulatory"
Clinical Regulatory Affairs - 17 Years of Experience - Near 30024
Tags for this Online Resume: regulatory affairs, clinical coordinator, atlanta, Quality Assurance, documentation, time management, orginazation
Clinical Regulatory Affairs - 20 Years of Experience - Near 55311
Summary of Specialized Skills * Design, development and conduct of device based Clinical and Pre-Clinical Research projects. * Experience in writing various clinical documents, including protocols, CERs, reports, research findings. * Design and Implementation of various Pre-clinical trials for pilot studies of various implantable technologies. * Management of scientific/animal studies and clinical projects. * Hands-on exper...
Tags for this Online Resume: Imaging, Cardiology, Integrated Development Environments, Management, Data Management, PACEMAKER, Pacemakers, Research, Clinical Research, Publications
Clinical Regulatory Affairs - 20 Years of Experience - Near 53143
Summary 30 plus years in the Medical Device and Pharmaceutical industry. Extensive expertise in Supply Chain, Customs Compliance (import and export), Test methods and Process Validations, Technical product development and support, GTIN and UDID process for organizations that meet GS1 standards. Experience in Customs Compliance and Quality Systems Regulations as well as domestic and international standards. Core competencies...
Tags for this Online Resume: Customs Compliance, Scrum Master, Regulatory Affairs, Validation, HR, Quality, Compliance, Hepatitis, Planning, Quality Assurance, Project Manager, Medical devices
Clinical Regulatory Affairs - 5 Years of Experience
Profile Regulatory Affairs Specialist with more than five years of experience in the pharmaceutical and biotechnology industries, implementing global regulatory filing strategies. Education in biotechnical engineering with deep knowledge and practical skills in managing the submission process from start to end, monitoring and tracking information, communicating with colleagues, managers and subject experts for efficiency an...
Tags for this Online Resume: Manufacturing, Packaging, Pharmaceutical, Regulatory Affairs, Biotechnical, Filing, Management, Medical, Medical Devices, Microsoft Office
Clinical Regulatory Affairs
Clinical Regulatory Affairs - 20 Years of Experience - Near 37221
Tags for this Online Resume: Business Development, Business Planning, Business Strategies, Cancer, Computer Aided Software Engineering, Consulting, Critical Care - Neurology, Distribution, Documentation, Drafting
Clinical, Regulatory and Medical Writing
Project Manager
SUMMARY Experienced IT Software professional specialized in working with clients to understand and implement requirements and applications/systems to provide business analytics and strategic solutions in various roles as a Senior Business Analyst, Senior Project Manager, Senior SFDC Architect, Senior Program Manager/Product Manager and Senior Product Owner. Collaborate with product management, engineering and other cross-fu...
Ideal Companies: program mgnt
Tags for this Online Resume: Inventory, Support, Active Server Pages, Forecast, Forecasting, Oracle, Quality, Quality Assurance, Data Entry, Planning
Clinical Regulatory Affairs - 3 Years of Experience - Near 60462
Tags for this Online Resume: Sales, Training, Arabic Language, English Language, Good Clinical Practices, International Sales, Management, Operational support systems, Presentation Skills, Regulatory Affairs
Clinical Regulatory Affairs
Regulatory Affairs
Aspiring to work with a growing organization that offers a challenging environment where I can learn and carve a niche for myself and effectively contribute to the organizations target and aspirations. Firmly believe that imagination, passion and boundless curiosity always set levels and standards that exceed expectations.
Tags for this Online Resume: Computer Literate, Manufacturing, Microsoft Excel, Microsoft PowerPoint, Microsoft Word, Packaging, Diagnostics, Evaluate, Filing, Its
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
