Clinical Research Coordinator - Dept Of Surgery Embedded
Phoenix, AZ, United States
USD 50K-83K (estimate) Mid-level Full Time
Tasks
- Coordinate clinical research protocols
- Ensure regulatory compliance
- Identify and report adverse events
- Maintain protocol documents and amendments
- Manage research data quality and compliance
- Monitor research activities and subject participation
- Obtain IRB approval
- Prepare and submit IRB documents
- Provide education and training to department staff
- Screen enroll and recruit research participants
Perks/Benefits
- Comprehensive health benefits
- Continuing education opportunities
- Dental insurance
- FSA
- HSA
- Retirement plan
- Vision insurance
Skills/Tech-stack
Adverse Event | Adverse event reporting | Clinical Research | Data Management | Event Reporting | Human subjects research | IRB compliance | Interventional study coordination | Medical terminology | Protocol amendment management | Regulatory Compliance | Study coordination
Education
Associate Degree | Bachelor of Science | High School Diploma
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