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Online Resumes with "Human Subjects Protection"



Clinical Research Project Manager, Charlotte North Carolina

To acquire a mid level to managerial administrative position within the clinical research therapeutic field

Tags for this Online Resume: regulatory, data manager, project manager, quality assurance, auditor, monitoring, electronic data capture, GCP, research, eCRF, CCRP, human subject's protection, source documentation, study start up, primary outcome analysis

Featured Profile

Analyst

Tags for this Online Resume: writing, Institutional Review Board, clinical trials, regulatory, human subject protections, specialist

Clinical Research 14 years experience

My objective is to use my extensive knowledge of clinical research, FDA, ICH, and GCP guidelines to obtain a career in the Pharmaceutical/Biotech industry.

Tags for this Online Resume: Clinical Reserach, IRB, Human Subject Protection, Audit, Monitor

Featured Profile

Director, Business Development Clinical Research IRB- 14 years Experience- Seattle/Portland/Denver

Senior marketing and client development executive with 14 years experience in clinical research. I am looking for continued growth as a research professional leading project teams and staff in support of strategic business goals. As a leader in the development and maintenance of productive client relationships, I have been recognized for expanded customer utilization of products and services with a focused customer-centric...

Ideal Companies: Quintiles, Huron Consulting, Roche, Genentech, PharmaLink Consulting, Icon, Covance, PRA International, AAHRPP

Tags for this Online Resume: Account Management, Client Services and Develpment, Marketing, Project Management, Presentations, Budgeting, International Business, Team Leadership, Process Improvement, Training/Development, Performance Management, Business Development, Operations Management, Branding, Vendor Relations, Clinical Research Regulatory Compliance, Federal Regulations

Director, Human Research Protections - 17 Years Experience - Institutional Review Board Management - Human Subjects, Regulatory Education Development - Research Management, Department of Defense

I'm a Human Subjects Protection professional who has over 17 years of experience in managing research and regulatory programs. Extensive knowledge of regulations, writing and implementing policies and procedures, review of all study documents, training and development of staff, conduct of consent processes, subject education, and study monitoring.

Tags for this Online Resume: Institutional Review Board, Human Subjects Protection, Director, Manager, Department of Defence, Universtiy, Medical Center

Director - 20 Years of Experience - Near 90732

AREAS OF EXPERTISE NEW BUSINESS DEVELOPMENT, MARKETING & SALES BUSINESS MANAGEMENT & CONSULTING PROJECT BUDGETING & MANAGEMENT STRATEGIC ALLIANCES FINANCIAL PERFORMANCE HUMAN SUBJECTS PROTECTION RESEARCH E-COMMERCE STRATEGY BUSINESS & STRATEGIC PLANNING NEW PRODUCT DESIGN/LAUNCH * Strategic planning and operations improvement in fast paced business environments to increase strategic alliances, revenues, marketing and sales ...

Tags for this Online Resume: Business Development, e-Commerce, Electronic Commerce, Health Insurance, Insurance, Managed Care, Management, Management Information Systems, Marketing Management, Business Development Consultant Management New Product Development

Clinical Research - 1 Years of Experience - Near 60091

Leverage Masters and Medical Degrees in clinical trials for new drugs and medical devices.

Tags for this Online Resume: AMICUS, Phlebotomy, Medical, Research, Cancer, clinical trials, regulatory, phase iii, phase ii, pharmaceutical, IRB, eCRF, Rave, ICF, Clinical Protocol, IB, Apheresis, Hematology, Leukemia Trials, GCP, Human Subject Protection, Medicine, HIPPA, Responsible Conduct of Research