TI Clinical Research Assistant II

• Perform on-site visits with research subjects, including obtain informed consent, perform research procedures including vital signs and specimen collection, document visits, and enter data. Maintain documentation for research protocol. • Support data abstraction and entry for both the NW NTM Biobank, the Bronchiectasis Research Registry, and other NTM-related protocols. Abstraction will be done mainly via Epic EMR, but other databases could be utilized. • Complete special projects under the guidance of one of the group epidemiologists, including manuscript review, database support, administrative support for clinical trials, etc. • Bachelor's Degree in relevant field OR • Associate's AND • 2 years of relevant experience OR • 3 years of relevant experience OR • Equivalent combination of training and experience • Strong written, verbal comminication and proficeincy in MS Office Suite; meticulous record keeping and organization skills. • Working knowledge of IRB guidelines and FDA, DHHS, other agency guidelines that govern clinical research. • Experience with EndNote or other citation software. • Ability to perform the job duties with or without accommodation. • Bachelor's degree in Public Health or • Masters Degree in Public Health or currently working toward Masters Degree in Public Health • 1-2 years of experience in clinical research including at least 1 year of clinical trial coordination • A working knowledge of FDA, • DHHS, IRB and other agency guidelines that govern clinical research. • Experience working with Epic, or other EMR systems. • REDCap database • Familiarity with OHSU’s CTMS (OnCore) • Good Clinical Practice (GCP) Certification, SOCRA or ACRP Certification Phlebotomy training • Bachelor's Degree in relevant field OR • Associate's AND • 2 years of relevant experience OR • 3 years of relevant experience OR • Equivalent combination of training and experience • Strong written, verbal comminication and proficeincy in MS Office Suite; meticulous record keeping and organization skills. • Working knowledge of IRB guidelines and FDA, DHHS, other agency guidelines that govern clinical research. • Experience with EndNote or other citation software. • Ability to perform the job duties with or without accommodation. • Bachelor's degree in Public Health or • Masters Degree in Public Health or currently working toward Masters Degree in Public Health • 1-2 years of experience in clinical research including at least 1 year of clinical trial coordination • A working knowledge of FDA, • DHHS, IRB and other agency guidelines that govern clinical research. • Experience working with Epic, or other EMR systems. • REDCap database • Familiarity with OHSU’s CTMS (OnCore) • Good Clinical Practice (GCP) Certification, SOCRA or ACRP Certification Phlebotomy training