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For your reference, we have included the original job posting below.
Senior Clinical Research Associate
Job Number:
72579903
Company Name:
Covance
Job Location:
US
Job Categories:
Healthcare & Medical Sales & Sales Management
Senior Clinical Research Associate
We are looking for talented professionals with the clinical industry to join us as Senior Clinical Research Associate in Australia. If you have 4 years & above of CRA experience and global trial experience, we would love to speak to you on ourSenior Clinical Research Associateopportunity.
Covance is committed to providing a career with purpose in a culture that values achievement. By joining our Clinical Development Services (CDS) team, you will work in a collaborative environment and giving you an excellent overview of best practices across the industry. Covance Clinical Development Services is based on an integrated clinical development services that is unique to Covance as we are one of the few truly global drug development companies positioned to provide comprehensive clinical support from First-in-Human studies through pivotal Phase III global clinical ut the job:Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assignedPrimarily responsibilities of a Clinical Research Associate: * Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned * Responsible for all aspects of site management as prescribed in the project plans * Recruitment of potential investigators, submissions preparation, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor * Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned * Complete Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs * Independently perform Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management
