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Online Resumes with "health authorities"



DATA MANAGEMENT ANALYST - 4.5 YEARS EXPERIENCE - Bangalore India

To work learn and grow with an organization to reach a high level in Regulatory Submission Management hierarchy and be instrumental in driving it beyond its mission by adhering to its values and cultures and utilizing my potential and talent to its fullest.

Tags for this Online Resume: Regualatory Publishing, Regulatory Affairs, Submission Manager, Health Authority , ISI Tool Box, eCTDXpress, ISI Publisher, Liquent, Insight Publisher, CMC Documentation, USFDA, EMEA, MHRA

Pharmacovigilance/Drug Safety - 13 Years of Experience - Near 19380

Pharmacovigilance professional with over 10 years experience in product safety roles of increasing responsibility seeking further career growth opportunities

Tags for this Online Resume: Argus Experience, Pharmacovigilance, Validation, adverse event managment, submission to health Authorities

Physician - 20 Years of Experience - Near 18000

In reviewing my CV against the Professional Qualification Requirements of the Health Authority it appears that I'm currently qualified for the Specialist Physician in Gulf region. EDUCATION 1.Master of Medical Sciences in Anaesthesiology since 2000 2.Specialist in Anaesthesiology and Reanimatology since 1995 3.Professional exams, Advanced university degree since 1988 4.Doctor of Medicine (M.D.) ...

Tags for this Online Resume: Master of Medical Sciences in Anesthesiology, Specialist in Anesthesiology and Reanimatology, General Anesthesia, Spinal and Epidural, Chronic Pain Management , TICI and TIVA, Peribulbar and Subtenon blocks, Total Parenteral Nutrition

Clinical Regulatory Affairs - 13 Years of Experience - Near 19711

My background includes 13 years’ experience in the Pharmaceutical Industry at AstraZeneca Pharmaceuticals in Global Regulatory Submissions and Life Cycle Management of Regulatory documents. This includes 6 years’ experience as a Project Manager for Regulatory Global submissions. As a Project manager within the Submission Management Group, I provided expertise on global submission compilation and published electronic submiss...

Tags for this Online Resume: Newark, DE, Life Cycle Management, Regulatory Global Submissions, Pharmaceutical Industry, RSS Application, eCTD Publisher, electronic submissions, Regulatory Publisher, Management, Cardiovascular, Document Management, Legal, Pharmaceutical, Project Management, Publishing, Quality Assurance

Medical Referral Coordinator 3 years experience,

To continue to work with community in the private or public sector. Have alot to contribute with ten years with Los Angeles Unified School District, Labor & Indusstries, Industrial Insurance Sector, and then with the Puyallup Tribal Health Authority.

Sales Manager - 16 Years of Experience - Near 92649

Sales Executive/Manager with many years of experience selling multi-million dollar contracts for hardware, software, consulting and professional services to enterprise clients. I possess a “Hunter” mentality, and am a results-oriented, high-energy sales and business development professional. I am highly skilled managing the sales process from account development to closing sales. My clients included IBM, Sun Microsystems...

Tags for this Online Resume: Sales, Software, Unix, SAN (Storage Area Network), Services, Account Manager, Disaster Recovery, Patient Education

Clinical Research - 10 Years of Experience - Near 18901

Summary: * Several years of clinical experience in the industry with excellent knowledge of drug development in different therapeutic areas including oncology, immunology, vaccines, metabolism and biosimilars. Solid clinical practice experience. * Many years of Drug Safety, pharmacovigilance, risk management and epidemiology experience * Experience interfacing with health authorities (worldwide), institutional review boards...

Tags for this Online Resume: Oncology, Protocol, Regulatory Affairs, Risk Assessment, Management, Risk Management, Risk Management Activities, Complaints, Documentation, Hematology, Medical Affairs, Clinical Development

Team Leader - 9 Years of Experience - Near 08854

Experience Summary * A seasoned analytics and consulting professional with ~9 years of industry experience as a SAS Consultant and Business Data Analyst with a strong understanding of Data Handling and Management, SAS, Project management, and Business Analysis. Project Summary This program supports the in-out of the company's innovative value-based programs. This includes the analyses of business KPIs and financial metrics ...

Tags for this Online Resume: Programming, Support, ETL, QA, Management, Data Extraction, Project Management, Requirements Analysis, SAS, Data Analyst

Director

Dedicated and Strategic QA Professional with more than fifteen years of progressive experience in both large and small pharmaceutical companies both US based and international. Extensive experience in development through commercialization of solid oral dosage products. Comprehensive knowledge of cGXP and ICH guidelines. Leader of process and manufacturing compliance, document control programs, QA analytical sciences, vali...

Tags for this Online Resume: Internal and External Audits, Vendor Management, Quality Systems, CAPA, Customer Complaints, Chemistry Machine Control

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 - 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

Clinical Pharmacovigilance/Drug Safety - 10 Years of Experience - Near 19440

Summary Clinical Scientist/Clinical Data Analyst/Clinical Data Management/Project Coordinator/GLP auditor/Research Biologist with over 15 years experience in the pharmaceutical industry. Authored/QC review of protocols, protocol amendments, protocol clarification letters, informed consent forms, risk language, periodic safety reports (PSUR, DSUR, QSR), investigator brochures, medical monitoring plans, clinical SAE narrative...

Tags for this Online Resume: Protocol, Oncology, Audit, Monitoring, Critical Care - Neurology, ICH, Neurology, Quality Assurance, Test, Data Quality