Oncology Regulatory Coordinator for Cancer Trials

St Luke; Boise (ID); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

On-site massages

Employee Assistance Program

Wellness tools

Career development

Job summary

St. Luke’s invites applications for a Research Regulatory Coordinator to navigate FDA, IRB, and ICH GCP requirements in oncology trials. The role focuses on regulatory submissions and documentation to advance breakthrough cancer care.

Join a mission-driven team at St. Luke’s that values accuracy, collaboration, and growth, with comprehensive benefits and steady professional development.

Qualifications

• 2+ years of regulatory experience in oncology or complex therapeutic area clinical research
• Experience with FDA/ICH GCP and IRB submissions is strongly preferred
• Ability to manage multiple studies and coordinate regulatory activities across sites

Responsibilities

• Prepare, manage, and track regulatory submissions for oncology clinical trials
• Maintain essential documents and ensure every study meets high ethical, safety, and compliance standards
• Collaborate with investigators, sponsors, and multidisciplinary oncology teams to keep trials moving forward
• Serve as a trusted regulatory guidance resource across early- and late-phase and disease-specific cancer studies

Skills

Regulatory experience

Oncology

FDA

ICH GCP

IRB submissions

IND safety reports

Regulatory submissions

Multisite coordination

CTMS

eReg systems

IRB platforms

Communication skills

Regulatory guidance

Tools

CTMS

eReg systems

Electronic IRB platforms

Job description

St. Luke’s invites applications for a Research Regulatory Coordinator to navigate FDA, IRB, and ICH GCP requirements in oncology trials. The role focuses on regulatory submissions and documentation to advance breakthrough cancer care.

Join a mission-driven team at St. Luke’s that values accuracy, collaboration, and growth, with comprehensive benefits and steady professional development.