Cancer Clinical Research Coordinator Associate - Breast

Cancer Clinical Research Coordinator Associate - Breast (Hybrid) jobs in United States

Stanford University School of Medicine

• Biotechnology

Responsibilities

• Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through closeout
• Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies
• Coordinate collection of study specimens and processing
• Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms
• Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure Institutional Review Board renewals are completed
• Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact
• Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff
• Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct
• Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements
• Participate in monitor visits and regulatory audits

Preferred

• Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred

Benefits

• Hybrid work schedule
• Glassdoor
• 4.0
• Stanford Medicine improves health through leadership, diversity and collaborative discoveries and innovation in health care, education and research.
• Stanford, California, USA
• https://med.stanford.edu/scgpm.html
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Qualifications

• Knowledge of the principles of clinical research and federal regulations
• Familiarity with IRB guidelines and regulations
• Previous experience with clinical trials
• Two-year college degree and two years related work experience or a bachelor's degree in a related field or an equivalent combination of related education and relevant experience
• Strong interpersonal skills
• Proficiency with Microsoft Office
• Knowledge of medical terminology
• Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred

Required skills

• California Class C Driver’s License, Clinical Research, Clinical Trials, Federal Regulations, IRB Guidelines and Regulations, SoCRA or ACRP Certification

Preferred skills

• Written and Verbal Communication

Experience

• 2+ years