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For your reference, we have included the original job posting below.
Clinical Research Associate
Job Number:
42644219
Company Name:
Kforce
Job Location:
Pittsburgh, PA US
Job Category:
Management & Business
Clinical Research Associate
At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philosophies. Using these tools, Kforce is able to better plan and anticipate work loads and thus minimize the peaks of work that can swamp you. This allows you to stay just as dedicated and still strike a balance between work and home.
Currently, one of our top clients is in search of an exceptional Clinical Research Associate in Pittsburgh, PA. The role of the Clinical Research Associate (CRA) is to collaborate in the identification and drive the selection of investigator sites with input from other cross-functional groups. The CRA also monitors investigator sites in compliance with company SOPs, ICH / GCP and local laws so that site performance targets are achieved.
A few specific accountabilities: * Conduct SCV and ensure clinical trials data are submitted to data management in a timely fashion * Identify issues that may impact on the conduct of the study and ensure appropriate closure of all issues * Proactively manage a greater investigator site workload commensurate with experience so that studies are run efficiently and key study objectives are met * Ensure studies are run in line with ICH/GCP, local laws, and company SOPs and procedures * Ensure patient safety is maintained and all safety issues are reported correctly according to all relevant local and international regulatory requirements * Inform the PI and site staff of all issues * Agree and develop corrective and preventative actions with PI and site personnel to close all open issues * Be responsible for all aspects of site management from collaboration on site selection to study closeout
