Research Assistant (On-Site) – Phoenix, Arizona
Location: Phoenix, Arizona
Employment Type: Full-Time | On-Site
Job ID: R1510125
About the Role
This fully on-site Research Assistant position in Phoenix, Arizona is an excellent opportunity for professionals seeking to begin or advance their career in clinical research. The role is ideal for candidates who are passionate about healthcare, teamwork, and patient-focused clinical studies. While clinical skills such as drawing blood, measuring vitals, or performing EKGs are advantageous, they are not mandatory for selection.
You will contribute to the execution of clinical trials in alignment with all regulatory and protocol requirements, supporting research teams, clinical staff, and study participants throughout the trial lifecycle.
Key Responsibilities
Build and maintain productive working relationships with study teams, investigators, and clinic staff.
Assist with the screening, recruitment, and enrollment of study participants.
Manage participant scheduling, follow-up coordination, and clinical visit preparation.
Collect participant medical history and support data entry and data management activities.
Coordinate laboratory procedures and protocol-related follow-up tasks.
Support the informed consent process in accordance with IRB-approved protocols.
Uphold participant safety and ensure compliance with GCP/ICH guidelines and internal SOPs.
Ensure all visits and procedures are scheduled accurately as per study timelines.
Assist with maintaining documentation and clinical trial master files.
Required Skills and Qualifications
Understanding of GCP/ICH guidelines and basic regulatory requirements.
Knowledge of medical terminology preferred.
Clinical skills (vitals, phlebotomy, EKG) are beneficial but not required.
Strong interpersonal skills with exceptional attention to detail.
Ability to think logically, prioritize tasks, and adapt to changing study needs.
Proficiency in MS Office applications (Outlook, Word, Excel, PowerPoint, SharePoint).
Familiarity with clinical trial documentation systems is an advantage.
Experience Required
0–2 years of experience in clinical research, healthcare, or a patient-facing environment.
Fresh graduates with relevant educational backgrounds are encouraged to apply.
About the Employer
IQVIA is a global leader in clinical research, healthcare analytics, and life sciences solutions. The organization delivers data-driven insights and advanced clinical development services that support the innovation and commercialization of medical treatments worldwide.
Compensation
Annual base pay range: $29,400 – $73,400
Actual compensation will align with skills, experience, location, and schedule.
Eligible roles may include bonuses, incentives, and comprehensive health and welfare benefits.
Equal Opportunity Statement
IQVIA is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, veteran status, or any other protected classification.
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