Clinical Research Site Director - Phoenix, Arizona

MissionHires; Phoenix (AZ); On-site; USD 90,000 - 130,000; Full time

Job summary

MissionHires is seeking a dedicated Clinical Research Site Director based in Phoenix, Arizona. This role involves overseeing all clinical operations, managing staff, and ensuring high-quality trial execution while maintaining compliance with regulatory and financial standards.

The ideal candidate will have over 5 years of clinical research experience, including leadership, and must be fluent in both Spanish and English. Join us to drive forward our clinical research capabilities!

Qualifications

• 5+ years of clinical research experience with 2+ years in leadership roles.
• Deep understanding of ICH-GCP and FDA regulations.
• Experience in budget negotiation and oversight.

Responsibilities

• Lead and manage clinical research staff and operations.
• Develop and implement SOPs to ensure GCP compliance.
• Interface with sponsors and CROs during feasibility and study start-up.
• Ensure recruitment goals, timelines, and budget targets are met.
• Monitor quality metrics, audits, and CAPA plans.
• Direct all site operations.

Skills

Clinical research management

Budget negotiation

Fluent in Spanish

GCP compliance

Job description

Macoa Health is looking for a driven Clinical Research Site Director who is fluent in Spanish and passionate about expanding clinical research capabilities. The Site Director will oversee all clinical operations, supervise staff, and ensure high-quality trial execution while maintaining regulatory and financial compliance.

Responsibilities

• Lead and manage clinical research staff and operations.
• Develop and implement SOPs to ensure GCP compliance.
• Interface with sponsors and CROs during feasibility and study start-up.
• Ensure recruitment goals, timelines, and budget targets are met.
• Monitor quality metrics, audits, and CAPA plans.
• Direct all site operations.

Requirements

• 5+ years of clinical research experience, including 2+ years in leadership.
• Deep understanding of ICH-GCP, FDA regulations, and site operations.
• Experience in budget negotiation and financial oversight.
• Fluent in Spanish and English.