Cancer Clinical Research Project Manager Data Quality and Study Start-Up

$84,856 - $97,021/Yr

Stanford University - Stanford, CA

Full-time - Mid Level

Remote - Stanford, CA

251-500 employees

Educational Services

About the position

The Cancer Clinical Research Project Manager (CCRPM) at Stanford University will oversee data management integrity and the study start-up process within the Stanford Cancer Institute. This role is crucial for ensuring the successful implementation of cancer clinical trials, collaborating closely with physician investigators and clinical research staff. The CCRPM will manage significant aspects of clinical research study data entry, analysis, and training, contributing to the mission of reducing cancer mortality through comprehensive research and treatment.

Responsibilities

• 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.
• Audit operations to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes.
• 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.
• Ensure regulatory compliance and regularly inspect study documents.

Requirements

• Bachelor's degree in a related field.
• Two years of experience in clinical research or an equivalent combination of education and relevant experience.
• Strong interpersonal skills.
• Proficiency with Microsoft Office and database applications.
• Experience with research protocols and regulatory or governing bodies, including HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices.
• Knowledge of medical terminology.

Nice-to-haves

• Knowledge of clinical trials data management, clinical quality management, and study start-up processes.
• Clinical knowledge in the field of Lymphoma.
• Knowledge of various projects and implementation strategies.

Benefits

• Comprehensive health insurance
• Retirement savings plan
• Paid holidays
• Flexible scheduling
• Professional development opportunities