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Posted: Wednesday, September 20, 2017 6:45 AM

Req ID:12689
Shift: Days
Employment Status:AP : Active : Regular : Part Time
Job Summary 13;
The Violence Prevention Initiative at The Childrens Hospital of Philadelphia (CHOP) is seeking at Research Assistant to support a study evaluating a brief intervention for youth who have experienced violence:related injuries. Under the direct supervision of the study team, this individual will provide administrative and operational support to the research study.

Responsibilities will include but not be limited to participant recruitment and enrollment, administering study measures, scheduling participant visits, data entry, medical record abstraction, and study enrollment support. Additional responsibilities will include participation in project related meetings, literature reviews, and manuscript development. Candidates must be comfortable interacting with participants in the field (i.e. homes, schools, neighborhood settings), and perform well in office:based settings.
Job Responsibilities 13;
Provides technical and clinical support for day:to:day activities of research project according to the scope of work and timeline.
Perform medical record abstraction
Enter and manage subject data using RedCAP
Assist in enrollment procedures: screen and recruit participants in clinical and community settings to participate in research study; determine eligibility based on inclusion/exclusion criteria and conduct consent procedures; conduct study procedures and assessments according to study protocol.
Meet all quality assurance and confidentiality guidelines for data collection, and ensure accurate completion of questionnaires and other data collection during study visits
Schedule follow:up procedures for research participants with multiple time points.
Distribute participant incentives as needed.
Maintain master enrollment lists and tracking logs
Filing and office organization
Report adverse eventsPerforms specific administrative research duties according to work plan and priorities set forth by project leadership.
Provide direct administrative support to Investigators and Study Coordinator.
Assist with the development of summary reports, annual reports, evaluations, or other products.
Assist in the development of research protocols, amendments, project:specific databases, IRB continuing reviews, and sponsor reports.
Compile bibliographies, conducts literature searches and other investigative processes for the preparation of manuscripts, abstracts, etc.
Attend all meetings related to project, as requested
Initiates and maintains effective relationships with the project investigator(s), research team members and collaborators, the project sponsor, and participants and families.
Ensures that study team is kept up to date on all relevant activities within the research study.
Develop and maintain relationships with on:site staff and other key players involved in the study to ensure that participant burden is kept to a minimum and to enhance participant retention.
Conducts patient and family interactions in a professional and courteous manner.
Communicates effectively and professionally via electronic, telephone, and in:person modalities with diverse audiences

Required Licenses, Certifications, Registrations 13;
Education, Experience and Cert/Lic 13;
Education: Bachelors Degree in related field
Additional Technical Requirements 13;


• Location: South Jersey

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