Clinical Research Operations Leader - Multi-Site Manager

UC Irvine; California (MO); On-site; USD 90,000 - 150,000; Full time

Job summary

UC Irvine's Center for Clinical Research is seeking a Clinical Research Manager to oversee clinical research operations and staff across CCR locations. The role ensures adherence to study protocols and regulatory standards while managing budgets and vendor relationships.

The CRM will provide strategic guidance, coordinate with investigators, and supervise departments to maintain efficient trial progress. Travel to Irvine campuses may be required to support ongoing studies.

Qualifications

• Experience with study budgets, financial management, and billing oversight.
• Experience in training others in the field of research.
• Excellent verbal and written communication in a scientific environment.
• Ability to maintain confidentiality and interact with diplomacy.

Responsibilities

• Oversee clinical research operations across CCR and multiple sites.
• Lead staffing, onboarding, and workforce optimization.
• Ensure compliance with protocols, SOPs, and regulations.
• Provide high‑level analytical support for strategic initiatives.

Skills

Complex organizational structures

Research design

Study budgets

Personnel management

HR administration

Prioritization

Staff development

Communication skills

Stakeholder management

Regulatory compliance

Project management

FDA, GCP, ICH knowledge

Microsoft Office

Education

Bachelor's degree in related area

Research certification (ACRP, SoCRA, or equivalent)

7+ years of clinical research experience

Experience leading or supervising a team

Tools

Microsoft Office

Job description

UC Irvine's Center for Clinical Research is seeking a Clinical Research Manager to oversee clinical research operations and staff across CCR locations. The role ensures adherence to study protocols and regulatory standards while managing budgets and vendor relationships.

The CRM will provide strategic guidance, coordinate with investigators, and supervise departments to maintain efficient trial progress. Travel to Irvine campuses may be required to support ongoing studies.