Employers Only
  • Wheaton Franciscan Healthcare
  • Cisco
  • MillerCoors
  • Coventry Health Care
  • IBM
  • Liberty Property
  • Verizon Wireless
  • Rush University Medical Center
  • ServiceMaster
  • JPL
  • Federal Home Bank
  • Monsanto
  • Enterprise Rent A Car
  • Northrop Grumman
  • Yoh Company
  • Gwinnett Health Systems
  • Conoco Phillips
  • Methodist Hospital System
  • Johnson & Johnson Family of Companies
  • Kaiser Permanente
  • Wells Fargo
  • Mission Hospitals
  • Nestle USA
  • National Security Agency
  • TD Ameritrade
  • PwC
  • Ryder System
  • Parsons
  • Yum! Brands
  • WellPoint

Kaiser Permanente

Research Nurse Coordinator


Job Information

Posted:

Friday, January 18, 2013

Modified:

Tuesday, February 12, 2013

Division:

Northern California

Salary: 

0

Location: 

Oakland California USA

Job ID:

152174 (Kaiser Permanente Job ID)

HireDiversity Job ID:

3561971

Job Text


This position is responsible for the overall conduct of all research studies, & the supervision of all clinical research staff.
Essential Functions:
- Develops procedures & interprets policy
- Assures that all studies are conducted in accordance w/regulations established by KFHP, state, & other regulatory bodies
- Recruits & selects new clinical research staff
- Orients new research staff
- Counsels & disciplines staff members who are non-compliance w/applicable policies, procedures & standards
- Develops & implements clinical staff training & professional development programs
- Prepares research grants for submission & provides annual reports for CRC & IRB
- Monitors & reviews research study budget throughout fiscal year
- Maintains communications, coordinates & conducts site visits w/study sponsors
- Conducts regular staff meetings w/research staff
- Assures the proper documentation of all patient visits, site visits, meetings
- Assures and maintains strict adherence to protocol inclusion & exclusion criteria
- Participates in research data management
- Coordinates research patient recruitment
- Monitor for & assures that appropriate action for patients exhibiting adverse reactions during course of research study
- Provides nursing support of clinical studies as needed
- Develops protocol, analysis, & compilation of study results, teaching, publication, & other professional activities

Secondary Functions:
- Responsible for assisting in the informed consent process, screening potential patients for adult oncology clinical trials; assessing treatment patients for toxicities; dose modifications, and serious adverse events.
- Patient/family/medical/nursing staff education; assist physicians' in tumor assessments of subjects as per protocol.
- Assist in accurate data collection, and ordering all protocol requirements and obtaining results; preparation, collection, and shipment of all required protocol specimens.
- Attend National Research meetings as needed.

Qualifications:

Basic Qualifications:
- Previous adult medical nursing, clinical research, clinical management experience
- Previous supervisory experience
- Bachelor's degree in nursing
- Current California Registered Nurse License
- BLS certified
- Demonstrated professional competency
- Must be able to work in Labor and Management Partnership environment

++NOTE: This job is in adult oncology. Home base will be Oakland. Travel to other sites as needed for research activity/patient coverage. Must be willing and able to travel within the Northern California region with own dependable transportation. ++





External hires must pass a background check/drug screen.
We are proud to be an equal opportunity/affirmative action employer.

Save job

named

Share This Job!