IQVIA
healthcare
ClinicalResearchCoordinator
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“Clinical Research Coordinator at IQVIA. Skills: clinical research, study coordination, patient visits, data quality, patient safety, protocol adherence, data integrity. Perform clinical research procedures, including ECGs, vital signs, and biological sample collection. Coordinate day-to-day clinical research activities in accordance with study protocols and GCP requirements”
Industry & Context.
This position is not eligible for sponsorship
What They're Looking For.
Must Have
Minimum of 1+ years of clinical research experience, Ability to conduct patient chart review and prescreen subjects against inclusion/exclusion criteria, Experience independently leading subject study visits, Prior experience with EDC data entry and query resolution, Working knowledge of clinical trial conduct, GCP principles, and medical terminology, attention to detail
Nice to Have
Bachelor’s degree
What You'll Do.
Perform clinical research procedures
and biological sample collection
Coordinate day-to-day clinical research activities in accordance with study protocols and GCP requirements
Prepare study materials
and support logistical planning for research visits
and orient study participants while ensuring patient safety and protocol adherence
Lead and conduct subject study visits in alignment with protocol and investigator oversight
and document clinical data in case report forms (CRFs) and EDC systems
Collaborate with investigators
and site staff to resolve queries and maintain data integrity
Serve as a patient advocate and maintain a safe clinical environment consistent with Health & Safety policies
How You'll Work.
Team & Collaboration
Collaborate with investigators, study monitors, and site staff to resolve queries and maintain data integrity
Full Job Description
# **Clinical Research Coordinator - Anniston, AL** **Work Set‑Up:** 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 driving healthcare forward. We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. Our teams combine scientific expertise with cutting‑edge technology to deliver high‑quality clinical research that advances medicine. **About the Role** IQVIA is seeking a **Clinical Research Coordinator (CRC)** to support the execution of clinical research studies conducted under the supervision of a Principal Investigator. This role is ideal for a detail‑oriented, patient‑focused professional who thrives in a hands‑on clinical setting and is experienced in study coordination, patient visits, and data quality. **Key Responsibilities** * Perform clinical research procedures, including ECGs, vital signs, and biological sample collection * Coordinate day‑to‑day clinical research activities in accordance with study protocols and GCP requirements * Prepare study materials, set up equipment, and support logistical planning for research visits * Recruit, screen, prescreen, and orient study participants while ensuring patient safety and protocol adherence * Lead and conduct subject study visits in alignment with protocol and investigator oversight * Accurately collect, review, and document clinical data in case report forms (CRFs) and EDC systems * Collaborate with investigators, study monitors, and site staff to resolve queries and maintain data integrity * Serve as a patient advocate and maintain a safe clinical environment consistent with Health & Safety policies **Qualifications** * Bachelor’s degree preferred or an equivalent combination of education and relevant experience * Minimum of 1+ years of clinical research experience * Ability to conduct patien
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