Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Research Coordinator

Iqvia
IQVIA
1+ years
$43,500 – $72,500 per year
10 July 16, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Clinical Research Coordinator – Tempe, AZ (Full-Time)

Location: Tempe, Arizona
Job Type: Full-time
Compensation: $43,500 – $72,500 per year
Work Mode: On-site


Job Summary

IQVIA is seeking a dedicated Clinical Research Coordinator for its Tempe, AZ site. This is a full-time, fully on-site position for candidates with proven skills in clinical trial coordination, patient scheduling, informed consent, and specimen handling. The role requires familiarity with ICH-GCP guidelines, clinical operations, phlebotomy, and patient recruitment. As a CRC, you will support multiple low to moderately complex studies, collaborating closely with clinical and sponsor teams.


Key Responsibilities

  • Act as the primary CRC for 1–3 clinical studies of low to medium complexity

  • Perform patient screening, scheduling, data collection, and sample management

  • Obtain informed consent and support patient safety through protocol adherence

  • Manage investigational products and study supplies

  • Develop patient recruitment strategies and ensure enrollment targets are met

  • Collect patient history and vital signs including phlebotomy and ECG

  • Maintain source documents, enter clinical data, and resolve queries

  • Assist in monitoring visits and close-out activities

  • Coordinate pre-study and site qualification activities

  • Travel locally to other clinic locations as needed

  • Comply with IQVIA SOPs, GCP/ICH standards, and IRB protocols


Required Skills & Qualifications

  • Clinical Research Coordinator experience in a similar setting

  • Strong working knowledge of GCP/ICH guidelines and clinical trial procedures

  • Proficiency in clinical skills: vitals, phlebotomy, ECG, etc.

  • Knowledge of site operations and the drug development process

  • Strong organizational and communication skills

  • Competent with Microsoft Word and Excel

  • Ability to manage multiple studies under supervision


Perks & Benefits

  • Competitive annual salary range: $43,500 – $72,500

  • Bonus and incentive compensation opportunities

  • Health and welfare benefits package

  • Training and development in clinical research operations

  • Work with a global leader in life sciences and clinical trials


Company Description

IQVIA is a global leader in healthcare data science and clinical research, serving the life sciences industry. With a presence in over 100 countries, IQVIA helps accelerate the development of innovative medical solutions through analytics, technology, and research expertise.


Work Mode

On-site – Tempe, Arizona


Call to Action

If you're ready to grow your career in clinical trials and want to be part of a global leader in research, apply now to become a Clinical Research Coordinator at IQVIA in Tempe, AZ.