IQVIA
Healthcare
ClinicalTrialNurse
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Clinical Trial Nurse at IQVIA. Skills: Clinical trial execution, Patient care, Regulatory compliance. Perform clinical procedures. Collect biological samples”
Industry & Context.
Data query resolution
What They're Looking For.
Must Have
1+ year clinical research experience, Data entry experience, Query resolution experience, Good Clinical Practice knowledge, Clinical trial processes knowledge, Medical terminology knowledge, Phlebotomy experience, Medication administration experience, EDC systems proficiency, Accuracy in data management
Nice to Have
Bachelor's degree preferred
What You'll Do.
Perform clinical procedures
Collect biological samples
Coordinate clinical trial activities
Comply with protocols
Comply with site procedures
Prepare study materials
Maintain study documentation
Manage study logistics
Recruit study participants
Screen study participants
Consent study participants
Educate study participants
Ensure participant safety
Ensure protocol adherence
Collect clinical data
Document clinical data
Support monitoring visits
Support regulatory inspections
Act as patient advocate
Maintain safe research environment
Maintain compliant research environment
Engage in community outreach
How You'll Work.
Team & Collaboration
Collaborate with monitors; Collaborate with sponsors
Process & Methodology
Study coordination
Full Job Description
# **Clinical Trial Nurse – Augusta, GA** **Work Setup:** On-site **Schedule:** Part-time, 24 hours per week **About IQVIA** IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to advancing healthcare. We partner with leading pharmaceutical, biotechnology, and medical device organizations to accelerate innovation and improve patient outcomes. By combining deep scientific expertise with cutting-edge technology, we generate high-quality insights that drive the future of clinical development. **About the Role** IQVIA is seeking a **Clinical Trial Nurse** to support the successful execution of clinical trials under the direction of a Principal Investigator. This is a hands-on role that blends patient-facing care, clinical procedures, and study coordination responsibilities while ensuring strict adherence to regulatory and quality standards. **Key Responsibilities** * Perform clinical procedures including **phlebotomy, drug administration, ECGs, vital signs, and biological sample collection** * Coordinate day-to-day clinical trial activities in compliance with **protocols, GCP, and site procedures** * Prepare study materials, maintain study documentation, and manage study logistics * Recruit, screen, consent, and educate study participants while ensuring safety and protocol adherence * Accurately collect, document, and enter clinical data into **electronic data capture (EDC) systems** * Resolve data queries in collaboration with monitors and sponsors to ensure data integrity * Support monitoring visits, audits, and regulatory inspections * Act as a **patient advocate** , maintaining a safe and compliant research environment * Engage in community outreach efforts to support patient recruitment **Qualifications** * Bachelor’s degree preferred or an equivalent combination of education and relevant experience * **At least 1 + year of hands-on clinical research experience in a clinical or site setting** * Demonstrated
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