Clinical Trials Regulatory Affairs Coordinator (Hybrid)

US Oncology Network-wide Career Opportunities; Denver (CO); Hybrid; USD 65,000 - 95,000; Full time

Benefits offered by this job

Health, dental, and vision plans

Wellness program

Health savings account

Flexible spending accounts

401(k) retirement plan

Life insurance

Short-term disability insurance

Long-term disability insurance

Employee Assistance Program

PTO, holiday pay, tuition refund, and–

Employee paid critical illness and/or/

Accident insurance

Job summary

Rocky Mountain Cancer Centers in Denver is seeking an experienced Regulatory Affairs Coordinator to manage regulatory and administrative activities for clinical trials, ensuring compliance with USOR SOP, GCP, and applicable laws.

This hybrid role requires onsite work two days per week; candidates must reside in the Denver Metro area to support regular in-person collaboration and business needs. Minimum seven years in clinical research or regulatory affairs are expected.

Qualifications

• Associate's degree required; bachelor's in clinical or scientific field preferred.
• Minimum seven years of experience in clinical research, regulatory affairs or oncology.
• Experience with regulatory documents and SOPs is a plus.

Responsibilities

• Oversee regulatory and administrative activities for clinical trials with minimal supervision.
• Ensure compliance with USOR SOPs, GCP, and applicable regulations.
• Collaborate with research staff on QA initiatives and process improvements.
• May train other staff in regulatory processes.

Skills

Communication

Multi-tasking

Time management

Interpersonal skills

Attention to detail

Fast-paced

Education

Associate's degree

Bachelor's degree preferred

Tools

Microsoft Office

Job description

Rocky Mountain Cancer Centers in Denver is seeking an experienced Regulatory Affairs Coordinator to manage regulatory and administrative activities for clinical trials, ensuring compliance with USOR SOP, GCP, and applicable laws.

This hybrid role requires onsite work two days per week; candidates must reside in the Denver Metro area to support regular in-person collaboration and business needs. Minimum seven years in clinical research or regulatory affairs are expected.