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Job Title: Cancer Clinical Research Coordinator 2
Job Number:
Organization: Stanford
Posted: 9/11/2019
Type: Full-Time
Classification: Health Care - General
Industry: Academic Institutions
Number of Openings: 1
Location: Palo Alto,  CA    USA
Compensation:
Position Description: The Cancer Clinical Trials Office in the Stanford Cancer Institute, in Stanford University’s School of Medicine seeks a Clinical Research Coordinator 2 for the Breast Clinical Research Group to conduct clinical research and work independently on progressively more complex projects/assignments. Independently manage significant and key aspects of a few large complex studies.

Duties include: Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining participants in long- term clinical trials. Oversee data management for research projects. Develop and manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data. Develop project schedules, targets, measurements, and accountabilities, as assigned. Lead team meetings and prepare/approve minutes. Formally supervise, train, and/or mentor new staff or students, as assigned, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and performing related duties, in addition to instruction on project work. Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to requests and questions. Collaborate with principal investigators and study sponsors, monitor and report serious adverse events, and resolve study queries. Provide leadership in determining, recommending, and implementing improvements to policies/processes; define best practices. Develop study budget with staff and principal investigator, identifying standard of care versus study procedures. Track patient and study specific milestones, and invoice sponsors according to study contract. Ensure regulatory compliance. Regularly inspect study document to ensure ongoing regulatory compliance. Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are completed. * - Other duties may also be assigned

Qualifications: Experience working in Oncology Clinical Trials

Experience working on Investigator Initiated Trials

Organization Description: The Stanford Cancer Institute (SCI) is one of only 49 National Cancer Institute (NCI)-designated Comprehensive Cancer Centers in the country. As a NCI-designated Comprehensive Cancer Center the SCI is a dynamic and stimulating place to work as it maintains the highest level of scientific rigor, institutional support and coordination for the complete range of cancer-related research, including basic, translational, clinical and population-based science. The SCI brings together faculty with cancer-relevant expertise from four Schools and over 30 departments throughout the University. The Cancer Clinical Trials Office (CCTO) is an integral component of the Stanford Cancer Institute since the vital work performed there enables our cancer center to translate research from the laboratory into the clinical setting. Given the SCI’s mission, breadth, and depth it employs ~275 staff members (inclusive of the CCTO) in a fast-paced environment with tremendous opportunities for our Clinical Research teams.

Closing Date: 12/11/2019
Desired Starting Date:
Contact Name: Mandie Selin,  Cancer Clinical Research Coordinator 2
Contact Location:

    
United States
Contact Location:
 
      
  United States
Contact Phone:  
Contact Fax:
Contact Email: aselin@stanford.edu
Web Address:
How to Apply: https://careersearch.stanford.edu/jobs/cancer-clinical- research-coordinator-2-7310

Additional Information:

Web Site Delete Date: 12/11/2019