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Stanford, CA, United States
Source: Stanford University careers · View original posting
From Stanford University's posting. “We” and “our” refer to the employer.
Plan and administer both academic and research programs and services. Interpret principles and concepts generated by faculty, develop ideas and options for faculty review and decision, and then develop and implement instruction and research programs reflecting faculty interest. Special subject matter expertise in academic and/or research area is required for these jobs. Program management jobs without a research specialty may be better classified in Administrative Services Administrator series.
This position can operate within a remote work environment. The role may require occasional travel to clinical sites or partner facilities. The standard work week is 40 hours, with flexibility required during critical project phases.
The Division of General Surgery is seeking a strategic and results-oriented Project Manager to support initiatives within the Canary Center, Division of General Surgery, and Cancer Clinical Trials Office at Stanford University School of Medicine. Under faculty and research leadership, this role will develop, implement, and coordinate strategic programs focused on precancer research, clinical initiatives, and operational excellence.
The Project Manager will lead cross-functional projects from inception through completion, coordinate clinical, research, and administrative stakeholders, and ensure the timely and successful delivery of program goals.
Master's degree in cancer research or a cancer-related field. A Doctoral degree is preferred.
Minimum of 5 years of project management and regulatory experience in national and international oncology clinical trials.
Experience working with multidisciplinary research teams, patient engagement teams and multi-stakeholder panels; facilitating large-scale, multi-site grant submissions; and developing/maintaining national and international collaborations.
Familiarity with HIPAA, other healthcare regulations governing data security and patient care, and external regulatory processes.
Proven expertise in undertaking complex regulatory tasks:
Submitting IRB applications/amendments.
Compiling multi-site national/international Data Use Agreements (DUA) and Material Transfer Agreements (MTA).
Clinical trial reporting (clinicaltrials.gov).
Strong analytical, organizational and project management skills with the ability to synthesize and interpret research findings, manage budgets, and solve complex operational challenges.
Demonstrated ability to navigate complex clinical trial organizations, including cooperative group infrastructure, NIH organization, and structure of other trial sponsors and funders.
Exceptional written and verbal communication skills, with the ability to translate clinical needs into actionable project plans and integrate within an interdisciplinary research team.
Strong presentation skills including dissemination of knowledge products at national and international meetings.
Experience with relevant medical research databases and software.
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