Cancer Clinical Research Project Manager - Data Quality & Study Start- Up 103005 (Hybrid) 🔍School of Medicine, Stanford, California, United StatesNew📁Research📅8 hours ago Post Date📅103005 Requisition #Cancer Clinical Research Project Manager - Gyn-Onc (Hybrid)The Stanford Cancer Institute (SCI) is one of an elite number of National Cancer Institute-Designated Comprehensive Cancer Centers in the country, and is a prominent, dynamic, growing and complex Institute within the Stanford University School of Medicine. The SCI actively works to build synergies and collaborations among faculty with cancer-relevant expertise from four Schools and over 30 departments across Stanford University. Given the SCI's mission, breadth, and depth, it employs over 320 staff members in a fast-paced, team-oriented, and forward-thinking environment with tremendous opportunities for personal and professional growth. The Cancer Clinical Trials Office (CCTO) is an integral component of the Stanford Cancer Institute. The vital work performed there enables our adult and pediatric cancer centers to translate research from the laboratory into the clinical setting. You will be working with an unparalleled leading-edge community of faculty and staff who are fundamentally changing the world of health care in the cancer arena. We seek a Cancer Clinical Research Project Manager (CCRPM) to help us enact our mission to reduce cancer mortality through comprehensive cancer research, treatment, education, and outreach. Our CCRPM will provide oversight for data management integrity and study start-up process across a cancer clinical research group. They will independently manage significant and key aspects of clinical research study data entry, data analysis, and training of team members for all aspects of data quality. This position collaborates closely with physician investigators and clinical research staff to drive successful implementation of cancer clinical trials. Responsibilities include working with the research team(s), clinical staff, and Stanford Health Care departments to support conduct of safe and compliant clinical research. Reporting to the Gynecological oncology (Gyn-Onc) Clinical Research Manager (CRM), the CCRPM will be conversant in the goals, mission, and priorities of the Institute, and utilize this knowledge to ensure the safety and well-being of trial participants. We seek candidates with excellent interpersonal skills and attention to detail. Our staff run toward challenges, and you will have a demonstrated history of doing the same with a high degree of professionalism, initiative, and flexibility.
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