Clinical Research Associate Jobs in Oregon
A Clinical Research Associate (CRA) plays a pivotal role in the biotechnology industry, overseeing various aspects of clinical trials. These include designing, implementing, and monitoring clinical trials, ensuring data integrity, verifying case report forms, providing progress reports, and ensuring compliance with protocols and regulatory requirements. CRAs play a crucial role in the development, testing, and approval of new products in the biotechnology industry by managing the clinical trials that prove their safety and efficacy.
Important skills for a CRA include strong communication and organizational abilities, keen attention to detail, knowledge of clinical practices, and analytical skills. CRAs also need to be proficient in using specialized software for data analysis and trial management. Certifications such as Certified Clinical Research Associate (CCRA) or Certified Clinical Research Professional (CCRP) are typically required. Prior to becoming a CRA, individuals might have roles such as Clinical Research Coordinator, Clinical Trial Assistant, or Research Nurse, gaining necessary experience in managing clinical trials and working in a research setting.
trial coordination REDCap database Familiarity with OHSUs 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. + Conducting site visits to...
trial and regulatory experience Experience with Epic or other electronic medical records system Familiarity with the procedures of the OHSU Institutional Review Board Clinical skills, such as phlebotomy...
Remote WorkTherapeutic Interventional Senior Clinical Research Assistant
- Portland, OR
- 6 days ago
- Portland, OR
- 6 days ago
inclusion criteria for therapeutic interventional clinical trial....
IRB 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...
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 Oregon Health...
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....
In addition to our commitment to outstanding clinical care, we are also proud of our research programs from basic science research to clinical trials....
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....
Determine if clinical trial/study subject documentation aligns with the study hypothesis and monitor clinical trial/study safety in accordance with protocols, Good Clinical Practices (GCP), and regulatory...
Demographic Data for Oregon
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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 Housing Administration
- Mortgage Lending
- FHLMC
- Fannie Mae
- Sample Preparation
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Clinical Data Management
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Specimen Processing
- Biology
- Centrifuge
- Drug Development
- Site Management
- Biotechnology
- Physiology
- Clinical Trials
- Clinical Research
- Neuroscience
- Clinical Operations
- Oncology
- Medical Device Sales
- FDA Regulations
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Health Care
- Collections
- Auditing
- Investigation
- Written Communication
- Education Experience
- Quality Assurance
- Collaboration
- Documentation
- Reporting
- Bachelor's Degree
- Inventory Management
- Regulations
- Microsoft PowerPoint
- Policy Development
- Microsoft Office
- Problem Solving
- Research Skills
- Microsoft Excel
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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