Phase I Clinical Research Coordinator II/III

Arizona Liver Health; Chandler (AZ); On-site; USD 4,305,000 - 5,304,000; Full time

Benefits offered by this job

Health, Dental, Vision

PTO

Sick Time

Company holidays

401K with company match

Educational Assistance

Shared company vehicles

Job summary

Arizona Liver Health in Chandler, AZ is seeking a Clinical Research Coordinator II/III (Phase I) to support participant engagement, enrollment, and retention while ensuring compliant trial conduct. You will work under investigators to implement study protocols, manage data, and coordinate visits and adverse events.

The role requires training in clinical research, knowledge of FDA CFR and GCP, and strong interpersonal skills to collaborate with clinical teams, sponsors, and subjects in a

Qualifications

• Training appropriate to anticipated duties – Medical Assistant, associates, undergraduate, graduate degree or equivalent, study-specific training, other as applicable to assigned responsibilities.
• Experience and training in the conduct of clinical research (IRB submissions, reporting and source documentation, trial management).
• A thorough understanding of regulatory requirements, principles of GCP and biomedical research ethics.
• Interpersonal and communication skills—interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects and referral sources.

Responsibilities

• Develop and implement strategies to achieve Site Goals for participant engagement, enrollment, and retention.
• Build and maintain relationships with clinical teams, and other stakeholders at your facility
• Identify and monitor barriers to enrollment and retention and develop solutions to overcome them.
• Assist with training new staff members and assisting the site manager as needed.
• Ensure local strategies are successful through regular assessment and evaluations.
• Under the direction of the Principal Investigator or sub-investigator, manage the conduct of clinical research activities.
• Coordinate and implement assigned protocols in compliance with FDA CFR, GCP and company SOPs.
• May assume responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner.

Skills

Clinical research training

Regulatory knowledge

Interpersonal skills

Training background

Education

High school diploma or GED

Bachelor’s degree preferred

Job description

Arizona Liver Health in Chandler, AZ is seeking a Clinical Research Coordinator II/III (Phase I) to support participant engagement, enrollment, and retention while ensuring compliant trial conduct. You will work under investigators to implement study protocols, manage data, and coordinate visits and adverse events.

The role requires training in clinical research, knowledge of FDA CFR and GCP, and strong interpersonal skills to collaborate with clinical teams, sponsors, and subjects in a