IQVIA
Healthcare
ClinicalResearchCoordinator
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Clinical Research Coordinator at IQVIA. Skills: Clinical procedures, Study coordination, Data management. Perform complex clinical procedures. Coordinate clinical research studies”
Industry & Context.
What They're Looking For.
Must Have
High School Diploma or equivalent, 1 year of relevant work experience
Nice to Have
Phlebotomy pediatric experience, Experience with CRIO, Experience with Allscripts/Altera EMR
What You'll Do.
Perform complex clinical procedures
Coordinate clinical research studies
Maintain compliance with protocols
Conduct patient consenting
Process laboratory samples
Perform ABPM procedures
Prepare study materials
Plan logistical activities
Collect clinical data
Collaborate with investigators
Collaborate with monitors
Act as volunteer advocate
Maintain safe environment
How You'll Work.
Team & Collaboration
Collaborate with investigators; Collaborate with monitors
Full Job Description
# **Clinical Research Coordinator – Germantown, TN** **Work Set-Up:** On-site **Schedule:** Part-time, 24 hours per week ### ### **About the Role** ### We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance. Responsibilities also include working directly with consenting patients, conducting study visits, processing laboratory samples, and performing ambulatory blood pressure monitor (ABPM) procedures. Accurate and timely data entry will be an essential part of this role. ### ### **About IQVIA** ### IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials. ### ### **Key Responsibilities** * ### Perform a variety of complex clinical procedures, including ECG, spirometry, sample collection, and vital signs. * ### Phlebotomy is required; pediatric experience is highly preferred. * ### Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines. * ### Conduct patient consenting and perform study visits in accordance with study protocols. * ### Process laboratory samples and perform ABPM (ambulatory blood pressure monitor) procedures. * ### Support study conduct by preparing study materials, setting up equipment, and planning logistical activities. * ### Recruit, screen, and orient volunteers, ensuring their safety and well-being throughout the study. * ### Collect and accurately record clinical data
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