Senior Oncology Clinical Research Coordinator

SciBow; Palo Alto (CA); Hybrid; USD 72,000 - 92,000; Full time

Job summary

Stanford Cancer Institute is seeking a Clinical Research Coordinator 2 to support the Blood and Marrow Transplant/Cell Therapy programs. You will oversee recruitment, data management, budgeting, and regulatory compliance while mentoring staff and coordinating with investigators.

Ideal candidates have a bachelor’s degree in a related field and at least two years of clinical research experience, with strong knowledge of HIPAA, FDA regulations and GCP. This role is on-site at Stanford in Palo Alto.

Qualifications

• Bachelor’s degree in a related field and two years of experience in clinical research, or an equivalent combination of education and relevant experience.
• Experience with oncology clinical research, Blood and Marrow Transplant or cellular therapy is desirable.
• Knowledge of HIPAA, FDA regulations, IRB requirements and Good Clinical Practices.

Responsibilities

• Oversee subject recruitment and study enrollment goals and retention in long-term trials.
• Manage data for research projects, organize collect report and monitor data.
• Develop project schedules, lead team meetings, prepare minutes.
• Supervise/train staff and students, possibly hiring and evaluating performance.
• Audit operations for regulatory compliance and manage IRB submissions.
• Collaborate with investigators and sponsors, monitor adverse events and resolve queries.
• Develop and implement process improvements and best practices.
• Assist in study budget and invoice sponsors according to contract.
• Ensure regulatory compliance and INDA submissions when applicable.

Skills

Interpersonal skills

Microsoft Office

Databases

Regulatory knowledge

Medical terminology

Education

Bachelor’s degree in related field

Job description

Stanford Cancer Institute is seeking a Clinical Research Coordinator 2 to support the Blood and Marrow Transplant/Cell Therapy programs. You will oversee recruitment, data management, budgeting, and regulatory compliance while mentoring staff and coordinating with investigators.

Ideal candidates have a bachelor’s degree in a related field and at least two years of clinical research experience, with strong knowledge of HIPAA, FDA regulations and GCP. This role is on-site at Stanford in Palo Alto.