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Online Resumes with "REGULATORY "
Clinical Regulatory Affairs
Medical or Health Services Manager - 19 Years of Experience - Near 33319
I believe my extensive experience in the Directing, Administration and Operational Leadership make me an ideal candidate for this position. My primary expertise in Executive administration, Quality management, Compliance, Regulatory affairs, Public relations, Organizations, Coaching, Communication skills, Audit and Budget displayed over the years, boosted my qualifications.
Tags for this Online Resume: employment, newyork, connecticut, Policies and Procedures, Chemistry, Hematology, Immunology, Security, Management, Cms
Clinical Research - 16 Years of Experience - Near 34465
Karen.Sinkler@mail.com http://www.linkedin.com/pub/karen- Karen.Sinkler@mail.com http://www.linkedin.com/pub/karen- Provided oversight and leadership to clinical research sites throughout the U.S. 2
Ideal Companies: 1 month -
Tags for this Online Resume: Clinical Research, Monitoring, Management, Registered Nurse, Regulatory, Study Coordinating
Hotel and Resorts Finance and Operations Executive with over 20 years experience as VP, CFO, Corporate Controller, etc....
I am looking for a company to settle down and to grow with, a company I can be with for 30 years. On the flip side, am also open to contract and consulting work, also interested in pursuing this option as well as traditional permanent employment.
Ideal Companies: Hotel and Resort developers, Marriott, Starwood, etc.
Tags for this Online Resume: Hotel, resort, Real Estate, Controller, Director, General Manager, revenue, Budgets, forecast, performance, profit, condo, hoa, association, golf, restaurant
Clinical Regulatory Affairs
Safety Manager - 20 Years of Experience - Near 40475
Skills Summary * 15 years of product certification experience managing agency projects with multiple agency partners. * Review of proposed IECEE/CE Regulatory standards for US Tag for TC61. * Experience facilitating compliance with CE marking directives. * Development of compliance team and certification related processes. * 10 years' experience handling commercial cooking, commercial refrigerator and other related categori...
Tags for this Online Resume: Program Manager, Certified Senior Advisor, EMC, Packaging, UL, Management, 5S, ASTM, Compliance, ISO
Clinical Regulatory Affairs
Clinical Research Associate
SUMMARY: To apply my knowledge of FDA Good Clinical Practice guidelines/ICH guidelines, extensive site/field Clinical Director, Site Lead Study Management, in addition to my experience with various therapeutic areas of medicine, to a position as a Clinical Research Associate. AREAS OF EXPERTISE * Management * Interview candidates and either make a selection decision or recommend individuals for hire. * Able to manage multip...
Tags for this Online Resume: Clinical Research, Research, Accounting, Acquired Immune Deficiency Syndrome (AIDS), Advertising, Amazon Elastic MapReduce, Audit, Basic First Aid, BLS, Budgeting
Clinical Regulatory Affairs
Auditor - 11 Years of Experience
Keya is a currently a Senior Manager in the Advisory Services practice of Ernst & Young LLP. Her professional experience includes working on various internal audit engagements for clients in the insurance financial services shared services healthcare manufacturing and telecommunications sectors. Keya has over ten years of experience that includes risk based internal (operational regulatory compliance etc.) audits internal c...
Tags for this Online Resume: Audit, Internal audit, Inventory, Manufacturing, Receivables, HR, Human Resources, Accounting, Consumer Goods, Consumer Products
Clinical Research - 10 Years of Experience - Near M1T3N
SUMMARY: * NIH trained Study/Site Coordinator with 10 years of experience in clinical research coordination and administration. * Demonstrated ability in coordinating & implementing Network / Pharmaceutical / Investigator-driven multisite Phase I - IV clinical studies. * Adept in liaising with internal and external stakeholders.
Tags for this Online Resume: Protocol, Clinical Research Associate, Infectious Diseases, ICHGCP, Logistics of study material, Monitoring, Data Entry, Team Lead, Essential Documentation, Informed Consent, SOPs, Coordinator, Regulatory, QA/QC, Source Docmentation, CRF's, TMF, EDC, Toronto, Contracts, SAE
