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Online Resumes with "Clinical Regulatory"



Clinical Regulatory Affairs

Clinical Regulatory Affairs

Sr. Regulatory Affairs Mgr

Agricultural Technician

Clinical Research - 15 years experience - NJ

part-time work-at-home clinical data entry

Chief Compliance Officer - 22 years experience - Phoenix

Tags for this Online Resume: Phoenix, San Diego, Compliance Officer, Privacy Officer, regulatory affairs, genetics

Featured Profile

Biotech/Healthcare Research Professional/Associate with a PhD in Pharmacology and 10 years of progressive medical experience conducting research in science, healthcare, life sciences, toxicology, environmental health, lung cancer, and Non-Hodgkin’s lymp

I am a LifeScience/Biotech/Healthcare Research Professional with a PhD in Pharmacology and 10 years of progressive medical experience conducting research in science, healthcare, life sciences, toxicology, environmental health, lung cancer, and Non-Hodgkin’s lymphoma at four major medical centers. I am currently seeking employment as a Toxicologist, biotech equity research associate, or a LifeSciences/Biotech/ Healthcare/Med...

Ideal Companies: OrbiMed, Cowen and Company, Oppenheimer & Co. Inc., Bionest Partners, Leerink Partners, MLV & Co., Canaccord Genuity, GUGGENHEIM PARTNERS, CBPartners, Global Pharma, Pfizer, GuidePoint Global, Healthcare Group, A.T. Kearney, Accenture, Bain & Company, Bioinformatics LLC, Booz & Company, Booz Allen Hamilton, Boston Consulting Group, Deloitte, IMS Consulting Group, L.E.K. Consulting, McKinsey & Company, Monitor Group, Oliver Wyman, Opera Solutions, PricewaterhouseCoopers, Thomson Reuters, ZS Associates

Tags for this Online Resume: Occupational Health, Clinical trials, drug discovery, data analysis, Ph.D., financial models, consulting, healthcare, financial markets, epigenetics, lymphoma, research, research reports, investing, Biotech Research, Technical Support, Financial Statements, Market Analysis, Reporting, Life Sciences, Research Projects, Healthcare research, Presentations, Scheduling, Event Planning, Strategic Planning, Team Leadership, Team Motivation, Process Improvement, Outsourcing, Technical Writing, Training/Development, Workforce Planning, Client Relations, Pharmacology, Policy Development, Customer Service, Project Management, Oncology, Lung Cancer, Toxicology, Toxicologist, Analysis

Senior Quality Assurance / Labeling (Regulatory Compliance) Manager

I'm an Senior Manager / Director level professional with 17+ years' experience in medical device labeling, regulatory compliance, risk analysis, quality systems/CAPA, and process engineering. I regularly am enrolled in classes at Stanford University and enjoy other forms of professional development; see my profile at www.linkedin.com/in/aimeecampbell

Tags for this Online Resume: labeling, quality, FDA, CAPA, device, process engineering, translation, MDD, Health Canada, Menlo Park, SF Peninsula, San Francisco, manager, project, EU, DMR, Risk, DHF, analysis, implementation, operations, Director, team, leader

Senior staff scientist / Program Manager

Manage / implement a product stability program under current regulations; manage implementation of FDA requirements post 510(k) clearance

Ideal Companies: medical device companies; adjunct college professor; education manager within a company

Tags for this Online Resume: Product Quality Support, Product stability , medical device software validation, adjunct professor_biology

Chief Operating Officer (Clinical and Regulatory) at CRO and Consulting company

COO or Vice President Clinical And Regulatory Affairs at small to medium Biotech/Pharma

Tags for this Online Resume: COO, Pharmaceutical , Biotechs, Clinical studies, Regulatory, NDA

Manager, Regulatory Affairs and Quality Assurance - 9 years experience - NYC

Clinical Regulatory Affairs