Programmer I (Contract)
Covance (Sydney, NSW)
assigned by senior Statistical Programming staff. . Carry out all activities according to Covance SOPs working within the framework of the Quality Management System and to Good Clinical GCP). . Develop and review SAS programs and ...Notes are only visible to you.
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Senior Clinical Research Associate
Covance (Adelaide, SA)
review. Monitor data for missing or implausible data o Ensure the resources of the Sponsor and Covance are spent wisely by performing the required monitoring tasks in an efficient manner, according ... tasks as instructed by supervisor as ...Notes are only visible to you.
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Senior Clinical Research Associate
Covance (Adelaide, SA)
review. Monitor data for missing or implausible data o Ensure the resources of the Sponsor and Covance are spent wisely by performing the required monitoring tasks in an efficient manner, according ... tasks as instructed by supervisor as ...Notes are only visible to you.
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Senior Clinical Research Associate
Covance (Sydney, NSW)
review. Monitor data for missing or implausible data o Ensure the resources of the Sponsor and Covance are spent wisely by performing the required monitoring tasks in an efficient manner, according ... tasks as instructed by supervisor as ...Notes are only visible to you.
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Clinical Data Coordinator II
Covance (Melbourne, VIC)
Apply quality control procedures and checks to ensure data quality standards (client and Covance) are achieved . Potentially serve as a reviewer of project documents such as protocols, CRFs (or eCRFs monitoring conventions, CRF (eCRF) completion ...Notes are only visible to you.
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Specialist II, Global Site Services
Covance (Sydney, NSW)
process and track regulatory & investigator documents required for study site activation in accordance with Covance SOPs, sponsor SOPs, GCP ICH guidelines and the Investigator Package Plan ... contracts and budgets with investigative sites within parameters provided by ...Notes are only visible to you.
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