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Posted: Tuesday, July 18, 2017 11:01 AM


Req ID:11023
Shift: Any
Employment Status:AX : Active : Per Diem
Job Summary 13;
Under the direct supervision of the study team assists in the coordination of the details of the human research subject study and documentation concerning study protocols.
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Job Responsibilities 13;
:Providing technical and clinical support in the conduct of clinical studies
:Filing and office organization.
:Patient/research participant scheduling/history.
:Data collection; data entry; data management.
:Laboratory procedures.

:Consent subjects, with appropriate authorization and training.

:Research Study Compliance
:Adhere to an IRB approved protocols.
:Comply with Institutional policies, SOPs and guidelines.
:Comply with federal, state, and sponsor policies.

:May be called upon to:
:Document and Report adverse events.
:Maintain study source documents.
:Complete case report forms (paper and electronic data capture). 13;
Job Responsibilities (Continued) 13;
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Job Responsibilities (Continued) 13;
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Required Licenses, Certifications, Registrations 13;
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Required Education and Experience 13;
Required Education:: AA in a related field

Required Experience: 1+ year(s) relevant clinical research experience
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Preferred Education, Experience and Cert/Lic 13;
Preferred Education: BA/BS in a related field
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Additional Technical Requirements 13;
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Source: https://www.tiptopjob.com/jobs/69574988_job.asp?source=backpage


• Location: South Jersey

• Post ID: 40233943 southjersey
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