TI Clinical Research Assistant II

Job description

• 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