TI Clinical Research Assistant

Data Management and Abstraction

• Data abstraction, entry and management for new and ongoing assigned clinical trials and databases (including REDCap).
• Maintenance and submission of patient data and preparation of assigned clinical trials for quality assurance audits and monitoring.

Specimen Processing

• Collection and processing of samples including, but not limited to, placenta, blood, urine, cervical/vaginal secretion, and amniotic fluid.
• Follow oral and written protocols to process placental tissue, blood, CSF and urine samples.

Clinical Trials Management

• Responsible for patient interactions as outlined in protocol and as delegated by supervisor or Principal Investigator.
• Perform participant interviews and study procedures including physical measurements (i.e., blood pressure, heart rate, respiratory rate, temperature, and specimen collection).
• Management of pregnant people’s participation in clinical research trials at OHSU and other affiliated sites including regulatory and policy regulations systems, maintenance and submission of patient data, evaluation of protocol activities, maintenance and preparation for quality assurance audits and management of investigational drugs.

• Bachelor's Degree in relevant field of research OR Associate's AND 3 years of relevant experience OR 4 years of relevant experience OR Equivalent combination of training and experience

• 1-year relevant research

  experience in a laboratory

  setting

• Women’s Health specific experience is preferred. 3-5

  years research experience preferred

• Clinical Trials experience

  strongly preferred