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Clinical Research Coordinator, On-Site, Elkhorn, Nebraska

0-2 years
$36,600 – $91,300
10 Sept. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Clinical Research Coordinator (CRC) – On-Site

Location: Elkhorn, Nebraska
Job Type: Full-time, Office-based
Job ID: R1494189

Overview

Join a collaborative, patient-centered team to support clinical research studies. The CRC will coordinate studies, ensuring compliance with protocols, sponsor requirements, GCP, SOPs, and local regulations. This role provides professional development opportunities and allows meaningful contributions to clinical research and patient outcomes.

Key Responsibilities

Study Coordination & Patient Interaction

Coordinate clinical research studies under the supervision of the Principal Investigator.

Assist as backup CRC on other studies as needed.

Develop and implement patient recruitment strategies to meet enrollment targets.

Obtain informed consent from research participants.

Collect patient history, vitals, and other clinical data.

Administer investigational products and manage study supplies.

Schedule study visits and follow-up appointments.

Ensure patient safety and report adverse events.

Data Management & Documentation

Collect and maintain source documentation.

Perform data entry, query resolution, and essential study document management.

Order and track supportive study supplies (contracts, lab kits, imaging, IXRS, etc.).

Comply with IRB-approved protocols.

Site Operations Support

Facilitate pre-study activities, site qualification, study initiation, monitoring, and close-out visits.

Collect, process, and ship laboratory specimens.

Perform special projects and travel to other clinic locations as needed.

Compliance & Communication

Adhere to Avacare and Sponsor policies, SOPs, and regulatory guidelines.

Maintain strong working relationships with study team members and stakeholders.

Complete all protocol-related training.

Qualifications

Education & Experience

Experience as a Clinical Research Coordinator preferred.

Clinical skills including phlebotomy, EKG, and obtaining vitals.

Knowledge of site operations, drug development, and clinical trial procedures.

Knowledge & Skills

Understanding of GCP/ICH and applicable regulatory guidelines.

Effective communication and teamwork skills.

Proficiency in Microsoft Word and Excel.

Ability to handle multiple tasks in a fast-paced environment.

Compensation & Benefits

Base Pay Range: $36,600 – $91,300 per year (may vary based on experience, qualifications, and location).

Potential incentive plans, bonuses, and comprehensive benefits including health and welfare coverage.

Employer

IQVIA – A leading global provider of clinical research services, commercial insights, and healthcare intelligence. Learn more at IQVIA Careers
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Equal Opportunity Employer: IQVIA provides equal employment opportunities regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other protected status.