Clinical Research Associate Jobs in Oregon
Primary focus will be subject safety and compliance with the prescribed protocol and Good Clinical Practice. The TI Sr....
trial coordination REDCap database Familiarity with OHSU's CTMS (eCRIS) Good Clinical Practice (GCP) Certification, SOCRA or ACRP Certification Phlebotomy training Additional Details Due to the unpredictability...
What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards....
Remote WorkIRB training Good Clinical Practice (GCP) certification Phlebotomy training Additional Details Monday-Friday; between 8:00 AM - 4:30PM (flexible and will vary depending on study needs) All are welcome...
Department Overview The TI Clinical Research Associate works directly under a principal investigator and/or Research Manager/Director....
Knowledge of institutional review board (IRB) processes for submitting, modifying, terminating and continuing review of human protocols. Understanding of best practices for clinical research....
Duties include: assisting with trial start-up activities, including corresponding with the OHSU Institutional Review Board (IRB), eCRIS and ensuring all appropriate training and documentation is complete...
We expect the Clinical Research Associate to work with the team to identify and resolve research issues, develop research ideas, and disseminate results....
Demographic Data for Oregon
Moving to Oregon? Find some basic demographic data about Oregon below.
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Oregon
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Oregon offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Associate position
- Federal National Morgage Association
- ICH GCP
- Clinical Data Management
- Clinical Monitoring
- FHLMC
- Study Management
- Sample Preparation
- Clinical Trial Management System
- Medical Affairs
- Compliance Monitoring
- Legal Drafting
- Institutional Review Board
- ICH Guidelines
- DNA Isolation
- Physiology
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- Good Clinical Practice
- Biotechnology
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- Education Experience
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- Bachelor's Degree
- Regulations
- Microsoft Office
- Microsoft Excel
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- Research Skills
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- Communication Skills
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