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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.
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;
Job Responsibilities (Continued) 13;
Required Licenses, Certifications, Registrations 13;
Required Education and Experience 13;
Required Education:: AA in a related field

Required Experience: 1+ year(s) relevant clinical research experience
Preferred Education, Experience and Cert/Lic 13;
Preferred Education: BA/BS in a related field
Additional Technical Requirements 13;


• Location: South Jersey

• Post ID: 40233943 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