Clinical Research Nurse

2 weeks ago


San Francisco, California, United States University of California , San Francisco Full time
Job Summary

This is a limited appointment position that will end 12 months after the start date. The successful candidate will be responsible for performing initial review and input of protocols at Site Committee, reviewing and editing of Medicare Coverage Analysis (MCAs), and creating CTSI CRC budgets. They will also develop nursing-related forms and workflows for protocols and train nursing staff and neuro-oncology fellows on role-specific protocol development. Post-protocol activation duties will include Phase I chart reviews and AE/SAE reporting, with an emphasis on teaching nursing and Advance Practice Providers the process.

Key Responsibilities
  • Develop and implement protocols for neuro-oncology clinical trials
  • Review and edit Medicare Coverage Analysis (MCAs) and CTSI CRC budgets
  • Develop nursing-related forms and workflows for protocols
  • Train nursing staff and neuro-oncology fellows on role-specific protocol development
  • Perform Phase I chart reviews and AE/SAE reporting
Requirements
  • Bachelor of Science degree in Nursing
  • Three to five years of neuro-oncology research or clinical trial experience
  • Prior experience in developing protocols for neuro-oncology clinical trials
  • Working knowledge of clinical or laboratory research, clinical trial recruitment, eligibility, protocol adherence, quality data submission, and adverse event reporting
  • Ability to effectively manage multiple priorities, prioritize projects, and meet the demands of a fast-paced and dynamic work environment
Preferred Qualifications
  • Previous nursing experience in a neuro-oncology setting for 5 years
  • In-depth knowledge of clinical research contracts and grants, clinical trial protocols, FDA regulations, and complex visit structures
  • Experience with database design and management, including relational databases, creating and linking tables, designing complex queries, macros, and forms for accurate data collection and analysis
  • Project management experience
  • Experience with SharePoint software
  • Experience in training research staff in oncology clinical trials coordination
  • Experience designing web sites and computer-based surveys
  • UCSF clinical research experience, including experience with electronic IRB submissions (iRIS) and UCSF Cancer Center (OnCore) patient tracking and data entry
  • APEX/EPIC Super-user experience
License/Certification
  • Current RN California License
  • Current AHA CPR Certification
  • Current AHA ACLS Certification
Equal Employment Opportunity

The University of California, San Francisco is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information.



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