Clinical Research Associate/Clinical Research Coordinator

Senior Clinical Research Associate

Responsibilities Assisting in the design and execution of high quality clinical studies in compliance with FDA and ICH requirements. Function as a primary liaison to clinical investigators/site staff. Identify, qualify, initiate, monitor and close out clinical sites. Co-monitor with CRO when issues arise with the site. Assist in the selection and oversight of Contract Research […]

Director, GCP

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 quality. Additional responsibilities include consultation […]

Clinical Research Associate/Clinical Research Coordinator

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 sites in the US to […]

Clinical research in Ukraine and Russia

NBScience ___________________________ providing smart solutions for clinical research industries NBScience – an independent private company offering to Clients wide range of services in the area of clinical research industry. NBScience is a full service local company . We offer for our Clients full service solutions related to the clinical part of the study. We can […]

Visiting Clinical Research Coordinator

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, clinic staff, UIC IRB office, […]