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Clinical Research Coordinator

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.