Multi-Site Clinical Research Leader

ActivMed Practices & Research, LLC.; Gilbert (AZ); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Health, dental, vision insurance

Life and disability insurance

401k with safe harbor match

Health Savings Account

Job summary

Alcanza Clinical Research is seeking a Clinical Site Manager to oversee multi-site study activities, ensure protocol and GCP compliance, and drive site performance. You will lead staff, monitor enrollment and timelines, and maintain quality data and documentation in line with ICH/FDA guidelines.

The role requires an Associate degree with 3+ years of clinical research experience; management experience is preferred and bilingual English/Spanish is a plus.

Qualifications

• Associate’s degree and a minimum of 3 years of clinical research experience, or an equivalent combination of education and experience.
• One or more years of management experience is highly preferred.
• Bi-lingual (English / Spanish) proficiency is a plus.

Responsibilities

• Oversee site performance and regulatory compliance.
• Support delivery expectations and meet study milestones, enrollment targets, budgets.
• Manage site staff, training, and performance to ensure study deliverables.
• Review dashboards and clinical trial systems to ensure timely data updates and coverage.
• Collaborate with investigators to ensure patient safety and client goals.
• Identify and mitigate risks; implement corrective actions as needed.
• Participate in management or site meetings; handle additional duties as required.

Skills

MS Office

EHR

Web applications

Typing 40 wpm

Time management

Communication skills

Interpersonal skills

HIPAA compliance

Problem solving

Independent work

Management experience

Education

Associate degree

Job description

Alcanza Clinical Research is seeking a Clinical Site Manager to oversee multi-site study activities, ensure protocol and GCP compliance, and drive site performance. You will lead staff, monitor enrollment and timelines, and maintain quality data and documentation in line with ICH/FDA guidelines.

The role requires an Associate degree with 3+ years of clinical research experience; management experience is preferred and bilingual English/Spanish is a plus.