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Online Resumes with "gcp"
To partner with a company that understands, values and leverages the clinical evidence generated from a robust Clinical Affairs Department.
Quality Assurance Specialist, Clinical Quality Assurance - 17 years of experience- SQA Active Member
Based on my extensive experience in a variety of Health care and Clinical Research companies, I am confident that I would be a great asset to any organization. My expertise includes quality review of documents, processes and systems, root cause analysis, and CAPA investigation. In addition, my projects have focused on the development of the internal/external audits and risk assessments, audits of final clinical reports, po...
Clinical research professional with over fifteen years experience. Washington University graduate with an MS in Clinical Research Management. Extensive knowledge in both clinical operations and personnel management. Interested in pursuing a career in clinical operations that will enable me to contribute my skills and knowledge, and to provide an opportunity for professional development and career growth.
To increase the reliability of clinical research outcomes through appropriate practice of GCP and HIPAA guidelines.
I'd like to use my people and organization skills to communicate compliance requirements to cross-functional departments emphasizing the legal obligation biotech/pharma has to regulatory agencies and patients in an organization who supports the Quality Systems.
Tags for this Online Resume: SDLC, Agile, Scrum, Java, Project Management, Oracle, 21 CFR Part11, GCP, HIPAA, HL7, Software Architect , CTO, Healthcare, Clinical Research , Offshore Development, Open source technology, EDC, RDC
Highly experienced and FDA trained auditor seeking GCP auditor assignments as a freelance/Independent/Contract GCP auditor only. My past and current experience, education and training can add value to your firms goal of accomplishing completed quality work.
To find a job with a reputable pharmaceutical company that utilizes my experiences in clinical research study start up and ICH-GCP regulatory guidelines to provide process improvements and create a competitive advantage for the company.
I am currently seeking a position which will allow me to demonstrate my qualities as a responsible and resourceful team player. My knowledge includes extensive experience in the healthcare and clinical research arena, compliance training and analyzing, training coordination, Learning Management System testing and training, process development and implementation management, medical billing processing management, inventory ...