Research RN-Surprise
Ironwood Cancer & Research Centers
- Location
- Surprise, AZ
- Job type
- Full time
- Posted
- Oct 5
- 12 days ago
Career path
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About the company
Ironwood Cancer & Research Centers
Medical practice · 501 to 1,000 employees
Ironwood Cancer & Research Centers has beautiful state-of-the-art integrated Cancer and Women's Centers, with locations strategically located throughout the Valley. Each one provides a superior cancer care environment with a full spectrum of cancer related services for patients. Our multi-disciplinary team approach includes surgical oncology, medical oncology, radiation oncology, women's centers, diagnostic imaging services, social service support, nutritionist, integrative services, and genetic counseling. Mission Statement: To serve the community by providing quality, comprehensive cancer care which respects the values and needs of each individual.
What you'll do
- Reviews studies for clinical and operational feasibility, along with the Investigator and Director of Research.
- Screens, consents, enrolls and follows study subjects and oversees the same by non-RN clinical research coordinators, ensuring protocol compliance and close monitoring while subjects are on study.
- Responsible for all data and source documentation, adverse experience reporting, and will assist Regulatory Specialist in the maintenance of complete regulatory files.
- Responsible for following departmental policies and assuring proper billing for research subjects.
- Assists as needed in preparing study for submission to IRB and ensures all regulatory documents are completed.
- Ensures that randomization procedures and blinding procedures, as applicable, are followed as per protocol guidelines.
- Ensures eligible patients are enrolled and that consent process is appropriate and in compliance with all standards.
- Responsible for quality data entry into sponsor’s database (electronic data capture systems or paper CRFs) and query resolution.
- Prepares, mixes and administers investigational product, as applicable.
- Ensures proper study drug administration, compliance and accountability, including receipt, storage and dispensing.
What you need
- Reviews studies for clinical and operational feasibility, along with the Investigator and Director of Research.
- Screens, consents, enrolls and follows study subjects and oversees the same by non-RN clinical research coordinators, ensuring protocol compliance and close monitoring while subjects are on study.
- Responsible for all data and source documentation, adverse experience reporting, and will assist Regulatory Specialist in the maintenance of complete regulatory files.
- Responsible for following departmental policies and assuring proper billing for research subjects.
- Assists as needed in preparing study for submission to IRB and ensures all regulatory documents are completed.
- Ensures that randomization procedures and blinding procedures, as applicable, are followed as per protocol guidelines.
- Ensures eligible patients are enrolled and that consent process is appropriate and in compliance with all standards.
- Responsible for quality data entry into sponsor’s database (electronic data capture systems or paper CRFs) and query resolution.
- Prepares, mixes and administers investigational product, as applicable.
- Ensures proper study drug administration, compliance and accountability, including receipt, storage and dispensing.
- Education: a bachelor's degree
Key skills
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Perks
- health/dental/vision
- life insurance
- 401K
See full description on company page, apply now