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Posted: Tuesday, July 18, 2017 11:19 PM


Req ID:11781
Shift: Days
Employment Status:AF : Active : Regular : Full Time
Job Summary 13;
Assists the Radiology Department in data processing of proton spectroscopy and tasks related to setting up data analysis for studies of brain growth and development during infancy and early childhood.
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Job Responsibilities 13;
1. Assist in all aspects of data collection for lab:approved protocols.
*Review protocols for technical consideration.
*Assist in scheduling evaluations.
*Greet and triage all study subjects/families.
*Perform various relevant measurements and tests.

2. Assist in other kinds of lab:approved protocols.
*Compile study data and assist in data entry and report preparation.
*Attend meetings of the research teams as needed to provide updates on progress and problems.
*Help carry out and follow:up on protocol decisions for individual projects.

3. Help maintain lab facility and equipment.
*Perform quality assurance procedures on all equipment daily or as needed.
*Assist in reviewing quality assurance results, and communicate with manufacturers to assure full and proper operation of equipment.
*Schedule and document routine maintenance and servicing of equipment.
*Monitor use of supplies and order new supplies as needed.
*Maintain day:to:day operations of the lab and keep the facility neat, organized and safe.

4. Attend lab staff meetings and other relevant conferences/seminars. 13;
Job Responsibilities (Continued) 13;
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Job Responsibilities (Continued) 13;
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Required Licenses, Certifications, Registrations 13;
None 13;
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Required Education and Experience 13;
:Bachelors degree in related field or 3 to 4 years related work experience 13;
Preferred Education, Experience and Cert/Lic 13;
Experience in clinical research and computers is preferable.
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Additional Technical Requirements 13;
* Successful performance in a high:intensity work environment.
* Excellent problem identification and problem solving skills.
* Flexibility.
* Knowledge of computers and appropriate software packages.
* Ability to handle multiple tasks.
* Excellent interpersonal communication, organizational and managerial skills.
* Current knowledge of GCP and ICH guidelines, Definitions and Reporting requirements for adverse events, IRB issues and guidelines, Elements of Informed Consent, FDA Codes, and Regulatory Issues. 13;

Source: https://www.tiptopjob.com/jobs/69728963_job.asp?source=backpage


• Location: South Jersey

• Post ID: 40705808 southjersey
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