Clinical Research Coordinator enrolling patients in orthopedic studies at Banner Health. Responsible for data collection and patient education within the research protocols.
EG
Onsite Assistant Clinical Research Coordinator – Asst. CRC
Posted yesterday
About the role
- Assistant Clinical Research Coordinator at Evolution Research Group. Participating in clinical research studies, ensuring adherence to protocols, and supporting regulatory requirements.
Responsibilities
- Monitor and ensure study data is collected following plan of care, guidelines and identified group resources
- Serve in rotation with assistant clinical coordinators and clinical research coordinators
- Serve as liaison between assigned clinical research coordinator and all clinical departments
- Participate in collaborative team efforts with other departments
- Discuss and administer Informed Consent Form
- Check and ensure that procedure areas are properly stocked with study supplies and equipment (i.e. blood tubes, kits, study flowsheets, ECG machines, BP cuffs, etc.)
- Assist assigned Clinical Research Coordinator review study schedules to ensure that study procedures are properly staffed
- Assist assigned Clinical Research Coordinator with the creation and/or review of study flowsheets to ensure study is conducted according to protocol requirements
- Anticipate, recognize, and resolve issues
- Reads and understands each protocol in which she/he is involve
- Follow established guidelines in the collection of clinical data and/or administration of clinical studies
- Performs all other duties as assigned
- Support adverse event reporting and informed consent administration
- Notify staff of abnormal results or incidents
- Ensure participant comfort and readiness for procedures
- Set up supplies and procedure areas per protocol
- Perform venipuncture, vital signs, ECG, and other assessments
- Communicate with participants to explain procedures and gather data
- Assist with patient care and emergency measures as needed
- Attend study initiation meetings and perform study-related tasks
- Provide high-quality care under pressure
Requirements
- Professional Licensure, Registration and/or Certification in a clinical or allied health field is required with a minimum of one-year clinical research experience.
- BLS and/or ACLS, phlebotomy and injections certifications preferred but not required
- Basic computer skills, including knowledge of Microsoft Office, are required
- Certified Clinical Research Coordinator (CCRC) preferred but not required.
- Bilingual Spanish is preferred
Benefits
- medical and dental coverage
- matching 401(k)
- paid time off
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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