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Online Resumes with "Clinical project manager"
Clinical Project Manager with 18 years of diverse site monitoring and study project management. I specialise in data trend analysis and are duel certified as a CRA and Site Auditor. Responsible for 5 direct reports.
Drug Development executive with extensive global project management experience including strategic planning, risk management and quality assurance seeking position to oversee all aspects of Clinical Development within organizations, globally and cross- functionally, to include Clinical Operations, Clinical Project Management and Clinical Outsourcing.
I am a seasoned Clinical Research Scientist, Scientific Writer and Regulatory/Medical Affairs Specialist with years of experience in the bio-pharmaceutical industry. I consider myself a unique, multifaceted individual with outstanding communications, team-building, planning, supervisory, interpersonal capabilities along with effective organizational abilities and exceptional presentational skills. I am seeking a position th...
To further my career in the clinical research field by working in a position which will allow me to continue to utilize my current skills and experience in the medical field, as a certified coordinator and as a manager, as well as providing me with the opportunity to advance by learning new skills and responsibilities. I would appreciate the chance to prove that over 7 years of site experience, conducting clinical trials, ...
A highly motivated professional, with clinical research experience in pharmaceutical, CRO, biotechnology and oncology clinic settings through Project Management, Clinical Research Associate, Clinical Trial Coordination and laboratory research roles across Phases 1 to 4 and various therapeutics including oncology, major depressive disorder, HIV and diabetes. Possessing excellent communication skills and a broad foundation o...
My objective is to support the goals of large and small Biotech/Pharmaceutical companies. Manage day to day operations, monitor activities, develop documents, set standards and lead cross functional teams to ensure quality standards, regulatory compliance and strategically move projects forward in the advance of human healthcare.
Associate Director PVG, 11 years CRO experience, Global Project Managment, Safety Listing/Coding Reviews, Data Trending
Advancement in CRO or Pharma in PVG or Clinical Project Management. I have extensive experience in safety listing/coding reviews and global project management.
Direct clinical experience as a Data Manager or Clinical Project Manager