Position Summary Under direction, provides research, data analysis and operational support to principal investigators and research coordinators for clinical research studies Job Responsibilities Coordinates the recruitment and enrollment of study participants. Assesses patient eligibility for inclusion in clinical trials. Ensures proper consent protocols have been followed for study participation. Assists with departmental mailings, including patient medical records. Ensures accuracy of recipient contact information and location for correct delivery. Conducts literature reviews and gains expert familiarity with protocols that will be used as templates. Assists in creation of study database. Manages and enters collected data into study database. Conducts qualitative coding and thematic analysis of study data. May perform statistical analysis of research data. Assists in the preparation of materials, submissions and renewals to the Institutional Review Board (IRB) or IACUC. Assists faculty in the preparation of grant submissions and associated documentation, which may include just-in-time documents, progress reports, routing forms, abstracts and manuscripts. Performs other related duties as directed. Education High School Diploma Experience Bachelor's degree is preferred. Approximately one year of related experience. Knowledge, Skills And Abilities Statistical and database management experience, including proficiency in SPSS and/or RedCap. Previous clinical research experience is helpful. Knowledge of medical terminology is helpful. Working Conditions/Physical Demands Standard office work #J-18808-Ljbffr
8+ years of handson experience in Pega BPM , with a focus on CSSA/CLSA level architecture and high-scale implementations.5+ years of professional Java/J2EE coding to build custom applications and integrations.Proven track record of deep Pega customization. Experience...
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