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Posted: Friday, August 25, 2017 7:54 AM


Job Summary 13;
Under minimal supervision, coordinates all clinical research activities within the scope of clinical research protocols.
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Job Responsibilities 13;
The CRC II performs all CRC core and additional responsibilities as detailed in the CRC I job description. The CRC II Also may be responsible for any of the following:
:Manage study finances including sponsor invoicing and resolving study subject billing issues
:Develop advertisement materials
:Act as liaison for research subject, investigator, IRB, sponsor, and healthcare professionals
:Document investigational product (drug/device) accountability
:Self monitor and self:audit responsibilities
:Develop informed consent document
:Maintain Clinical Trial.gov
:Develop Case Report Forms
:Assignments to include more complex studies 13;
Required Licenses, Certifications, Registrations 13;
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Required Education and Experience 13;
Required Education:: BA/BS in a related field
Required Experience: 3+ year(s) relevant clinical research coordination experience
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Preferred Education, Experience and Cert/Lic 13;
Preferred Education: MA/MS in a related field
Preferred Experience: 1+ year(s) relevant clinical research coordination experience
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Additional Technical Requirements 13;
Requires effective writing and communication, work as part of a team, ability to multitask
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Source: https://www.tiptopjob.com/jobs/71185595_job.asp?source=backpage


• Location: South Jersey

• Post ID: 43565463 southjersey
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