Clinical Research Coordinator - Glendale, Az

1+ years

$35.00 – $42.00 per hour

Arizona

10 Oct. 29, 2025

Job Description

Job Type: Part Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Research Coordinator

Location: Glendale, Arizona (Office-based)
Job ID: R1510787
Employment Type: Part-Time
Work Setup: On-site
Schedule: 40 hours per week
Additional Locations: Arizona

Overview

IQVIA is seeking a Clinical Research Coordinator to assist in the planning and execution of clinical research studies under the supervision of a Principal Investigator. This role involves phlebotomy, pediatric experience, and community outreach as key components. The ideal candidate will ensure protocol compliance, patient safety, and data quality throughout the study lifecycle.

Key Responsibilities

Clinical Operations

Perform complex clinical procedures such as ECGs, spirometry, vital signs, and biological sample collection.
Conduct phlebotomy (required) and manage pediatric patients.
Maintain compliance with Health and Safety policies and ensure participant well-being.
Serve as a volunteer advocate and address participant concerns proactively.
Report deviations from clinical practices to senior staff and ensure corrective measures.
Assist registered and unregistered staff in clinical coordination and patient care.

Study Coordination & Execution

Review study protocols, CRFs, and electronic data capture systems.
Participate in project meetings and coordinate study activities.
Prepare for study setup including labeling, documentation, and equipment readiness.
Plan logistics for all procedures and ensure adherence to study timelines.
Prepare and deliver study-specific materials, documentation, and volunteer instructions.
Troubleshoot operational or procedural issues during study conduct.
Participate in team huddles to ensure assigned daily tasks meet performance standards.

Data Management & Quality Assurance

Perform data entry, verification, and quality checks to maintain accuracy and completeness.
Support data query resolution to ensure compliance with study protocols.
Collaborate with investigators to document and report AEs and SAEs according to protocol.
Cooperate with study monitors and ensure availability during monitoring visits.
Maintain compliance with ICH-GCP and company SOPs in all study-related tasks.

Volunteer Recruitment & Management

Recruit, screen, and select volunteers according to study criteria.
Conduct participant orientation sessions detailing study purpose, procedures, and schedules.
Manage the administration and custody of investigational products in compliance with site SOPs.
Record and report clinical findings accurately in CRFs and other documentation systems.

Qualifications

Education & Experience

High School Diploma (or equivalent) with 1+ year of relevant clinical research experience.
Prior experience in a clinical research environment strongly preferred.
Required certifications and licenses per company, state, or regulatory standards.

Technical Skills

Strong working knowledge of clinical trial processes and Good Clinical Practice (GCP).
Understanding of protocols, consent forms, and study schedules.
Proficiency in performing clinical procedures and handling clinical data.
Sound knowledge of medical terminology.
Excellent attention to detail, organizational skills, and problem-solving ability.
Ability to build effective working relationships with investigators, patients, and team members.

Additional Requirements

Phlebotomy and pediatric experience are mandatory.
This position is not eligible for sponsorship.

Compensation

Base Pay Range: $35.00 – $42.00 per hour
Actual pay depends on education, experience, and location.
Additional benefits may include performance incentives, health and welfare programs, and bonuses.

About IQVIA

IQVIA is a global leader in clinical research, healthcare intelligence, and life sciences solutions. We combine data science, advanced analytics, and deep healthcare expertise to accelerate medical innovation and improve patient outcomes.

🔗 Learn more: https://jobs.iqvia.com
🌐 Equal Opportunity Employer: IQVIA is committed to providing equal employment opportunities regardless of race, gender, identity, disability, veteran status, or any other protected category.
🔗 https://jobs.iqvia.com/eoe

Application

Apply Now to join IQVIA’s mission of transforming healthcare through evidence-based research and innovation.

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Clinical Research Coordinator - Glendale, Az

Job Description

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