IQVIA

Healthcare

ClinicalResearchCoordinator

$0–0k Germantown, Tennessee, United States PART TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Clinical Research Coordinator at IQVIA. Skills: Clinical procedures, Study coordination, Data management. Perform complex clinical procedures. Coordinate clinical research studies”

Industry & Context.

Healthcare

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

Free ATS check

Applying for this Clinical Research Coordinator role?

Most applicants get filtered before a human reads their resume. See if yours makes the cut.

How to Apply on Workday

  • Workday has a multi-step form — save your progress after every section.
  • "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
  • Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
  • Job requisition numbers are useful when following up with HR by email.

ANONYMOUS · UNFILTERED

What do employees actually say about IQVIA?

Real rants from real employees. Read before you apply.

Read Company Rants →