Regional Clinical Research Leader

Arizona Arthritis; Rockville, Northern (MD, KY); Hybrid; USD 90,000 - 120,000; Full time

Job summary

Arizona Arthritis & Rheumatology Associates, P.C. is seeking a Regional Research Manager to lead clinical research staff across multiple sites.

The role entails direct supervision, training, and routine site visits to ensure adherence to protocols, budgets, and data quality while coordinating with physicians, sponsors, and vendors. You will oversee onboarding, implement CTMS workflows, monitor regulatory compliance, and drive enrollment goals.

Qualifications

• Bachelor’s Degree or equivalent.
• 2 years’ experience as clinical research coordinator.
• Subject Matter expert in clinical research and indications.
• Understands state and federal regulations governing medicine and privacy.
• Strong leadership and organizational skills.
• Excellent verbal and written communication.
• Will travel to regional offices daily.
• CRI/CCR C certification preferred but not required.

Responsibilities

• Travel daily to research sites to provide support and ensure productivity.
• Direct, supervise, and evaluate coordinators and assistants.
• Train and mentor new staff for success.
• Assign tasks to balance workloads across recruitment staff.
• Utilize CTMS weekly to track productivity and data quality.
• Monitor eSource data capture for data and query goals.
• Manage HR duties including interviews and reviews.
• Ensure compliance with SOPs, ICH-GCP, FDA regulations.
• Coordinate site operations and vendor/study onboarding.
• Provide ongoing support and escalate issues to leadership.
• Communicate with physicians, sponsors, and CROs to resolve issues.

Skills

Leadership

Communication

Training & Mentorship

HR responsibilities

Travel to sites

Education

Bachelor's Degree

Tools

Clinical Trial Management System

Job description

Arizona Arthritis & Rheumatology Associates, P.C. is seeking a Regional Research Manager to lead clinical research staff across multiple sites.

The role entails direct supervision, training, and routine site visits to ensure adherence to protocols, budgets, and data quality while coordinating with physicians, sponsors, and vendors. You will oversee onboarding, implement CTMS workflows, monitor regulatory compliance, and drive enrollment goals.