Clinical Research Coordinator, On-Site, Elkhorn, Nebraska

2+ years

$36,600 – $91,300

Nebraska City

10 Aug. 29, 2025

Job Description

Job Type: Full Time Education: Knowledge of Good Clinical Practice (GCP)/ICH guidelines and regulatory standards. 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

Job Title: Clinical Research Coordinator

Location: Elkhorn, Nebraska (Note: The original posting incorrectly listed Elkhorn, Wisconsin)
Job Type: Full-Time
Work Set-Up: Fully On-Site (Office-Based)
Job ID: R1494189
Availability: Also available in additional locations
Company: IQVIA

Position Overview:

Join a collaborative, patient-centered clinical research team where your work directly supports groundbreaking medical studies and improved patient outcomes. This role offers an opportunity to grow professionally while making meaningful contributions to clinical research. Ideal for a driven, organized, and compassionate individual seeking long-term growth in the clinical trials field.

Key Responsibilities:

Clinical Trial Coordination

Coordinate and manage clinical research studies under the supervision of a Principal Investigator.
Serve as a backup Clinical Research Coordinator (CRC) for other studies as needed.
Ensure all activities comply with study protocols, ICH-GCP, and Avacare and Sponsor SOPs.

Participant Management

Develop and execute patient recruitment strategies to meet enrollment targets.
Obtain informed consent from research participants.
Schedule and conduct study visits, follow-up care, and related clinical procedures.
Collect participant histories, perform basic clinical tasks (e.g., vitals), and ensure participant safety.

Data & Documentation

Perform data entry and resolve data queries in EDC systems.
Collect and maintain source documentation.
Order and manage supportive study supplies (e.g., lab kits, imaging manuals).
Support essential regulatory document collection and review.

Operational Support

Administer investigational products and manage inventory.
Facilitate site qualification, initiation, monitoring, and close-out visits.
Process, collect, and ship laboratory specimens.
May assist in special projects or travel to nearby clinics as needed.
Perform additional duties as assigned.

Qualifications:

Required:

Knowledge of Good Clinical Practice (GCP)/ICH guidelines and regulatory standards.
Computer proficiency, especially in Microsoft Word and Excel.
Effective written and verbal communication skills.

Preferred:

Prior Clinical Research Coordinator experience in a similar setting.
Hands-on clinical skills (e.g., obtaining vitals, phlebotomy, EKG).
Familiarity with site operations and the drug development process.

Compensation & Benefits:

Annual Base Pay Range: $36,600 – $91,300
(Actual salary will vary based on experience, qualifications, location, and schedule.)
May include bonuses, incentive plans, and a comprehensive range of health and welfare benefits.

About IQVIA:

IQVIA is a global leader in healthcare intelligence, clinical research services, and advanced analytics. We partner with life sciences companies to drive innovation and improve healthcare outcomes through smarter connections between data, technology, and people.
Learn more: https://jobs.iqvia.com

Equal Opportunity Employer:

IQVIA is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected status.
EEO Policy: https://jobs.iqvia.com/eoe

How to Apply:

Visit https://jobs.iqvia.com and search for Job ID: R1494189, or click Apply Now to begin your application.

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