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Clin Research Coordinator II - philadelphia, pennsylvania

Clin Research Coordinator II - philadelphia, pennsylvania

Ad id: 1302182203288573
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Date listed 1 week ago
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Req ID:17158Shift: DaysEmployment Status:AF : Active : Regular : Full TimeJob Summary 13;Under minimal supervision, coordinates all clinical research activities within the scope of clinical research protocols. Specifically, the school:based bullying prevention clinical research team of the Violence Prevention Initiative (VPI) at Childrens Hospital of Philadelphia (CHOP) is seeking a Clinical Research Coordinator to assist with multiple research and programmatic activities. The Coordinator will work under the supervision of the Administrative Manager and Principal Investigator, and collaborate closely with the teams Clinical Supervisors. He/she will be part of an interdisciplinary team of psychology researchers and clinicians, research staff, and trainees ranging from undergraduate students to post:doctoral fellows in the areas of psychology, social work, public health, education, and other related fields. Responsibilities will include: Coordination of research activities, such as regulatory activities, recruitment/informed consent and data collection procedures, and master list/tracking procedures; Serve as school/community liaison and program champion in partnering schools; Data management, such as development and maintenance of database and codebooks; Coordination of administrative activities such as petty cash, reimbursements, meeting/event planning and documentation; and Supporting funding proposals/manuscript preparation.. 13;Job Responsibilities 13;The CRC II performs all CRC core and additional responsibilities as detailed in the CRC I job description.The CRC II also may be responsible for any of the following:Coordinate research activities:Coordinate regulatory activities, including management of documents and submissions to regulatory authorities (e.g. IRB, School Districts, etc.) and/or other review/monitoring boards.:Register studies on, as appropriate:Coordinate and participate in recruitment and informed consent processes for study participants:Coordinate and participate in data collection and other protocol:related research procedures:Serve as school/community liaison and program champion in partnering schools in order to develop and maintain relationships, foster ongoing information sharing and problem:solving, handle scheduling and follow:up needed for research activities (recruitment, data collection, intervention times), etc.:Manage master lists of study participants and adhere to all participant tracking procedures (consent status, completion of measures, class/school/intervention status, etc.), including ongoing review and updating of documents:Prepare study documents, including protocols, consent forms, data collection forms, and intervention materials:Review, organize and appropriately file all dataData management:Maintain existing project databases, including coordination and tracking of data entry and data integrity checks and preparing databases for analyses:Create project:specific databases as needed using MS Excel, RedCap, SPSS, and other relevant software:Maintain database codebooksCoordinate administrative activities:Provide direct administrative support to the Administrative Manager and leadership team:Manage petty cash and stipends/participant research cards for study subjects as needed:Coordinate reimbursements (e.g., purchases, travel):Coordinate events as needed (e.g., meetings, conferences, consultant visits):Develop and disseminate updates, meeting agendas, minutes and other source documents:Assist in communication with consultants, vendors, collaborators or contacts at study sites:Maintain systems to track contacts, communications, progress, and other pertinent informationManuscript and Funding proposal preparation / submission:Participate in preparing funding proposals, including biosketches/curriculum vitae and other grant components:Assist with preparation of mSource:

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Last Updated on: February 23, 2018
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