Clinical Research Nurse Coordinator I, Oncology
About The Position
Under moderate supervision, the Clinical Research Nurse Coordinator I (CRNC-I) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRNC) responsibilities. The CRNC-I is responsible for the planning and delivery of patient and family-centered care utilizing the nursing process of assessment, diagnosis, planning, implementation, and evaluation within the context of clinical research. The CRNC-I will interface with the clinical team to facilitate communication, clinical decision-making, patient safety, and care coordination throughout protocol implementation. Study management including but is not limited to assisting in assessing feasibility of clinical research protocols, preparing materials needed for regulatory review and submission to the Institutional Review Board (IRB), identifying potential study participants, collecting research data/specimens, completing study records in an accurate and timely manner, participating in quality assurance audits, managing study materials and supplies, communicating across multiple teams, and archiving records in accordance with appropriate policies and procedures. The CRNC-I may also be responsible for development of source documents and/or case report forms and coordination of research/project team meetings. The CRNC-I is the first position in the Clinical Research Nurse Coordinator series.
Requirements
- Minimum one year of clinical research coordination experience or relevant clinical experience.
- Bachelor of Science degree in Nursing (BSN).
- Basic knowledge of key Microsoft Office programs (Word, Excel, PowerPoint).
- Demonstrate strong interpersonal skills.
- Able to communicate effectively both orally and in writing.
- Be detail oriented.
- Able to work under pressure in a fast-paced environment while managing multiple competing priorities.
- Working knowledge of human subjects’ regulatory requirements and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use Guidelines for Good Clinical Practice (ICH-GCP).
- Registered Nurse (RN) – California Board of Registered Nursing.
- Basic Life Support (BLS) certification
- Pediatric Emergency Assessment, Recognition, and Stabilization (PEARS) upon hire or must be obtained within six (6) months of hire with valid Pediatric Advanced Life Support (PALS).
Nice To Haves
- Clinical research experience in a hospital setting and/or pediatric clinical research experience.
- Ability to conduct informed consent.
- Working knowledge of Cerner or equivalent medical record system.
- Knowledge of sample identification, processing and storage.
- Association of Clinical Research Professionals Certified Professional (ARCP-CP), Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC).
- Certification in area of clinical specialty.
Responsibilities
- Providing coordinator support to multiple human subjects’ (clinical) research projects
- Performing all core Clinical Research Coordinator (CRNC) responsibilities
- Planning and delivery of patient and family-centered care utilizing the nursing process of assessment, diagnosis, planning, implementation, and evaluation within the context of clinical research
- Interfacing with the clinical team to facilitate communication, clinical decision-making, patient safety, and care coordination throughout protocol implementation
- Assisting in assessing feasibility of clinical research protocols
- Preparing materials needed for regulatory review and submission to the Institutional Review Board (IRB)
- Identifying potential study participants
- Collecting research data/specimens
- Completing study records in an accurate and timely manner
- Participating in quality assurance audits
- Managing study materials and supplies
- Communicating across multiple teams
- Archiving records in accordance with appropriate policies and procedures
- Development of source documents and/or case report forms
- Coordination of research/project team meetings
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
