Senior Clinical Research Nurse & Study Coordinator

GI Alliance; Peoria (AZ); On-site; USD 90,000 - 120,000; Full time

Job summary

GI Alliance seeks an Experienced Research Nurse to mentor staff and lead complex clinical trials within a growing research department. You will ensure protocol adherence, regulatory compliance, and high-quality data collection while collaborating with PIs and Sub-Is.

You will oversee study start-up and site operations, train Coordinators, assist with recruitment, manage adverse events, and maintain CTMS/EMR systems, fostering efficient, compliant trial execution across multiple sites.

Qualifications

• Must have 4–6 years of experience conducting complex therapeutic area clinical trials.
• RN or LVN license in applicable state.
• Urology-based clinical experience preferred.
• Knowledge of FDA, GCP, ICH and federal/state regulations.
• Proficiency with EMR and Practice Management systems.
• ACRP certification (preferred).

Responsibilities

• Support building the research department in scope, size, reputation, and professionalism.
• Lead recruitment of studies with central recruitment team.
• Maintain knowledge of FDA, GCP, ICH, and regulatory requirements.
• Obtain and maintain consent of patients with high ethical standards.
• Screen, interview, and perform exams including EKG, blood draw, vitals.
• Work with EMR and data management systems to complete data and source requirements.
• Oversee daily operations and training of staff; manage multiple studies.

Skills

Trial management

Mentoring

Regulatory compliance

Urology experience

Communication

Education

RN or LVN license

ACRP certification (preferred)

Tools

CTMS

EMR/Practice Mgmt systems

Job description

GI Alliance seeks an Experienced Research Nurse to mentor staff and lead complex clinical trials within a growing research department. You will ensure protocol adherence, regulatory compliance, and high-quality data collection while collaborating with PIs and Sub-Is.

You will oversee study start-up and site operations, train Coordinators, assist with recruitment, manage adverse events, and maintain CTMS/EMR systems, fostering efficient, compliant trial execution across multiple sites.