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
.
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.
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