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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.
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
:Develop Case Report Forms
:Assignments to include more complex studies 13;
Required Licenses, Certifications, Registrations 13;
Required Education and Experience 13;
Required Education:: BA/BS in a related field
Required Experience: 3+ year(s) relevant clinical research coordination experience
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
Additional Technical Requirements 13;
Requires effective writing and communication, work as part of a team, ability to multitask


• Location: South Jersey

• Post ID: 43565463 southjersey is an interactive computer service that enables access by multiple users and should not be treated as the publisher or speaker of any information provided by another information content provider. © 2017