97281 Clinical Research Coordinator 6 months contract-to-perm
Clinical Research Coordinator (Pediatric Hematology Oncology) needed for a 6-month contract-to-perm position.
Bachelor's degree or associates degree.
Four years relevant work experience, including clinical data management or research experience in clinical trial database setting.
Computer skills related to data management required.
Excellent skills in English (both verbal and written) required.
Prior Pediatric Hematology Oncology experience REQUIRED.
1.) Provides all professional level support for pediatric research studies involving human subjects. Assists in the design of studies. Develop, verify and implement procedures to accomplish research goals.
2.) Implement Pediatric Hem/Onc Research protocol & monitor/participant adherence to protocol. Take action to correct deviations or other problems. Verify accuracy of research data & monitor data control. Maintain IRB of protocol amendments safety reports /serious adverse events etcD.in compliance with applicable regulations.
3.) Establish patient/participation screening procedures. Obtain relevant medical information from patient clinic charts medical records. Maintain logs/progress reports to track both currently enrolled as well as follow up patient/participants. Maintain Drug accountability
4.) Determine data to be collected & develop forms collecting/summarizing data. Maintain clinical research computer data base design & management. Ensure data integrity and consistency in the computer database & written records.
5.) Establish /maintain contracts with patients/participants, health care providers, community agencies, study sponsors, Update appropriate agencies such as IRB etc. regarding current status of research project.
Job Description:
Develop research protocols, coordinate recruitment efforts, maintain quality control, reporting and analysis and coordination with the IRB for all studies pertaining to Pediatric Hematology Oncology. Responsible for the screening/obtaining pertinent medical records for clinical research patients. Develop case report forms and determine actual parameters to be collected. Develop flow sheet of study events. Develop data collection forms for pharmacokinetic studies and enter data. Monitor visits, audit documents, prepare study summaries, document dropouts, respond to audits, and prepare data for reports and publications. Serve as a liaison between those individuals in the internal departments and medical facilities that telephone for assistance and regarding patient related information. Develops & coordinate training programs for the study's Principal investigators.
Estimated Salary: $20 to $28 per hour based on qualifications.
Bachelor's degree or associates degree.
Four years relevant work experience, including clinical data management or research experience in clinical trial database setting.
Computer skills related to data management required.
Excellent skills in English (both verbal and written) required.
Prior Pediatric Hematology Oncology experience REQUIRED.
1.) Provides all professional level support for pediatric research studies involving human subjects. Assists in the design of studies. Develop, verify and implement procedures to accomplish research goals.
2.) Implement Pediatric Hem/Onc Research protocol & monitor/participant adherence to protocol. Take action to correct deviations or other problems. Verify accuracy of research data & monitor data control. Maintain IRB of protocol amendments safety reports /serious adverse events etcD.in compliance with applicable regulations.
3.) Establish patient/participation screening procedures. Obtain relevant medical information from patient clinic charts medical records. Maintain logs/progress reports to track both currently enrolled as well as follow up patient/participants. Maintain Drug accountability
4.) Determine data to be collected & develop forms collecting/summarizing data. Maintain clinical research computer data base design & management. Ensure data integrity and consistency in the computer database & written records.
5.) Establish /maintain contracts with patients/participants, health care providers, community agencies, study sponsors, Update appropriate agencies such as IRB etc. regarding current status of research project.
Job Description:
Develop research protocols, coordinate recruitment efforts, maintain quality control, reporting and analysis and coordination with the IRB for all studies pertaining to Pediatric Hematology Oncology. Responsible for the screening/obtaining pertinent medical records for clinical research patients. Develop case report forms and determine actual parameters to be collected. Develop flow sheet of study events. Develop data collection forms for pharmacokinetic studies and enter data. Monitor visits, audit documents, prepare study summaries, document dropouts, respond to audits, and prepare data for reports and publications. Serve as a liaison between those individuals in the internal departments and medical facilities that telephone for assistance and regarding patient related information. Develops & coordinate training programs for the study's Principal investigators.
Estimated Salary: $20 to $28 per hour based on qualifications.
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