Clinical Research Coordinator II/III - Multitherapeutic Trials

Arizona Liver Health; Peoria (AZ); On-site; USD 38,000 - 50,000; Full time

Benefits offered by this job

Health, Dental, Vision (with HSA plans

3 weeks PTO

5 days Sick Time

401K with 6% company match

Short & Long Term Disability

CEUs / Educational Assistance

Shared company vehicles for required旅游

Job summary

Arizona Liver Health is seeking a Clinical Research Coordinator II or III in Peoria, AZ. You will work under the PI to manage clinical research activities, ensure regulatory compliance, and coordinate protocol execution across studies.

The role includes data collection, patient assessments, recruitment, and liaising with sponsors and vendors. Ideal candidates will have 2+ years in late-phase trials, strong knowledge of GCP and regulatory standards, and experience in data management and study

Qualifications

• Minimum 2 years of experience as Clinical Research Coordinator for late-phase trials.
• Knowledge of regulatory requirements, GCP, and biomedical research ethics.
• Experience with data management and trial enrollment management.

Responsibilities

• Oversee conduct of clinical research activities under the PI or sub-investigator.
• Coordinate and implement protocols per FDA CFR, GCP and SOPs.
• Collect and record clinical research data, assist in patient assessments, scheduling, and study files.
• Develop management systems and prepare for study initiation.
• Recruit and screen potential participants and meet recruitment goals.

Skills

Clinical research knowledge

Regulatory compliance

Communication skills

GCP familiarity

Education

Associates or Bachelor's degree in healthcare, clinical research management, or related

Master’s degree (preferred)

Job description

Arizona Liver Health is seeking a Clinical Research Coordinator II or III in Peoria, AZ. You will work under the PI to manage clinical research activities, ensure regulatory compliance, and coordinate protocol execution across studies.

The role includes data collection, patient assessments, recruitment, and liaising with sponsors and vendors. Ideal candidates will have 2+ years in late-phase trials, strong knowledge of GCP and regulatory standards, and experience in data management and study