OpenSpecimen (Krishagni)
Clinical Research Scientist II
OpenSpecimen (Krishagni), Houston, Texas, United States, 77246
Preferred Education and Experience
Master’s degree in life sciences, nursing, public health, pharmacy, or other health related disciplines Experience in oncology, primary care, psychiatry, or cardiopulmonary clinical trials; with a common clinical trial enterprise system, such as, Oncore; in site monitoring; and in clinical research, population health, or genomics. Community health worker background preferred. Experience in healthcare, academic, biobanking or research environment. Competence in data cleaning techniques, OpenSpecimen (or other biobanking platforms), Research Electronic Data Capture software (REDCap), e-clinical works, and Microsoft Office. Responsibilities
Clinical Research
Help develop protocol development and translational roadmaps for commercially oriented faculty led projects Liaison with compliance and privacy officers Ensure research is conducted in compliance with IRB approved protocols Work with clinical staff and providers in consenting patients for research projects Work as a patient liaison and advocate in longitudinal studies, including follow-up
Data Curation
Support faculty and staff in data collection, quality control and curation Occasionally abstract or transcribe electronic medical record (EMR) data for research data warehouse under supervision of study investigators
Administrative
Performs other duties as assigned, including travel, ordering, coordinating meetings for clinical trial committees and research project teams
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Master’s degree in life sciences, nursing, public health, pharmacy, or other health related disciplines Experience in oncology, primary care, psychiatry, or cardiopulmonary clinical trials; with a common clinical trial enterprise system, such as, Oncore; in site monitoring; and in clinical research, population health, or genomics. Community health worker background preferred. Experience in healthcare, academic, biobanking or research environment. Competence in data cleaning techniques, OpenSpecimen (or other biobanking platforms), Research Electronic Data Capture software (REDCap), e-clinical works, and Microsoft Office. Responsibilities
Clinical Research
Help develop protocol development and translational roadmaps for commercially oriented faculty led projects Liaison with compliance and privacy officers Ensure research is conducted in compliance with IRB approved protocols Work with clinical staff and providers in consenting patients for research projects Work as a patient liaison and advocate in longitudinal studies, including follow-up
Data Curation
Support faculty and staff in data collection, quality control and curation Occasionally abstract or transcribe electronic medical record (EMR) data for research data warehouse under supervision of study investigators
Administrative
Performs other duties as assigned, including travel, ordering, coordinating meetings for clinical trial committees and research project teams
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