TI Clinical Research Assistant II
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