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Posted: Thursday, August 24, 2017 1:45 AM

Req ID:8524
Shift: Days
Employment Status:AF : Active : Regular : Full Time
Job Summary 13;
The Clinical Research Coordinator II position will primarily be responsible for all aspects of study coordination for designated studies conducted within the Division of Oncology.
:Responsible for the coordination of clinical research trials and other studies as assigned within the Neuro:Oncology section in the Division of Oncology.
:Assist in keeping relevant protocol and patient information updated in the Oncology Research Clinical Trial Management System.
:Participate in research team meetings, division:wide coordinator meetings and continued education and training within the CHOP Research Institute related to this role.
Expected to attend trainings on good clinical practices (GCP) and research related regulations and responsibilities within the institution and will be held accountable for adherence to all policies and procedures surrounding this process and for maintaining up to date knowledge on these policies from IRB, FDA, ICH, GCP, or other sources.
Job Responsibilities 13;
This role will work with minimal supervision by a Lead/Senior Coordinator or supervisor within the scope of clinical research protocols and participate in research activities that include:
:Chart abstraction, completion of case report forms, data clarification, data entry into electronic database and remote data entry system, ensuring appropriate source documentation is maintained
:Promptly report adverse events, unanticipated problems, and protocol deviations per protocol, sponsor, institutional and other regulatory guidelines
:Ensure adequate subject selection and enrollment of eligible subjects
:Work with clinical team and other research staff to order research procedures including research specimens.
:Communicate study noncompliance with Lead Coordinator and PI
:Process and ship research specimens
:Assist regulatory specialist with preparation, submission and maintenance of regulatory documents
:Prepare for and facilitate monitor visits and audits 13;
Required Licenses, Certifications, Registrations 13;
SOCRA or ACRP certification (1 yr) 13;
Required Education and Experience 13;
Bachelors Degree with minimum 2:3 years clinical research experience or a Masters Degree in Public Health (or related field) with at least 1 year clinical research experience.
Additional Technical Requirements 13;
Specific knowledge and skills::/h4:
:Value for research integrity and collaborative research
:Requires a high degree of flexibility of hours
:Excellent communication skills/Strong interpersonal skills
:Effective problem solving/critical thinking skills
:Strong organizational and time management skills
:Computer competency including knowledge and proficiency in Microsoft Office Suite and web:based programs
:Knowledge of Good Clinical Practice (GCP) preferred 13;


• Location: South Jersey

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