clinical research associate
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Responsibilities The CRA/CRC is responsible for the monitoring or auditing of all activities subject to the, “ICH Good Clinical Practice: Consolidated Guideline,” (GCPs), supporting client programs administrated by Watermark ensure project data and summary statements are of known and documented quality. Requirements Will be expected to travel extensively to study Read more
Responsibilities The Director, GCP will be required to oversee all and participate in, quality assurance auditing of all activities subject to the, “ICH Good Clinical/Laboratory Practice: Consolidated Guideline,” (GCP/GLP’s), supporting a program of quality assurance (QA) to ensure that Allergan project data and summary statements are of known and documented Read more
Responsibilities As part of this dynamic Cancer Center CTO team, Clinical Research Coordinators will manage & oversee several oncology clinical trials, from study inception to termination. Responsibilities for this position include but are not limited to: activation & maintenance of the oncology clinical trials protocols; acting as liaison between physicians, Read more
NBScience ___________________________ providing smart solutions for clinical research industries NBScience offering to Clients wide range of services in the area of clinical research industry. We offer for our Clients full service solutions related to the clinical part of the study. We can also take care about IMP and other Read more
Short List of Commonly Used Acronyms in Clinical Research 700U Statement of Economic Interest ACRP Association of Clinical Research Professionals AE Adverse Event ADR Adverse Drug Reaction AMA American Medical Association BID Twice Daily BIND BiologicalIND CAP Collegeof American Pathologists CBCTN Community Based Clinical Trials Network CBER Centerfor Biologics Evaluation and Read more
