IQVIA · 20 hours ago
Clinical Research Coordinator, On-site, Omaha, NE
Omaha, NE
Full-time
Onsite
Mid Level
$37K/yr - $91K/yrIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. The Clinical Research Coordinator will assist in the conduct of clinical trial activities, ensuring compliance with regulations and achieving study objectives through coordination and support of clinical research projects.
AnalyticsHealth CareLife Science
Responsibilities
Coordinates advanced clinical research projects as the primary CRC on at least 4 studies of medium to high complexity, as well as back-up CRC on other studies when needed
Assures that the integrity and quality of clinical research trials is maintained
Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved
Oversees the work of research assistants and trains junior staff as appropriate
Works effectively with multidisciplinary, ancillary, and inter-professional research teams
Functions independently, and is able to identify situations where additional support is necessary
Completes all protocol related training
Performs patient/research participant scheduling
Collects patient/research participant medical history
Collects and maintains source documentation
Manages inventory and administers test articles/investigational product to participants
Performs data entry and query resolution
Supports the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging, and laboratory handling manuals, etc.)
Adheres to an IRB approved protocol
Obtains informed consent of research subjects
Supports the safety of research subjects, report adverse events
Coordinates protocol related research procedures, study visits, and follow-up
Facilitates site qualification, study initiation, and monitoring visits, and study close-out activities
Ensures proper collection, processing, and shipping of laboratory specimens
May be asked to perform special project responsibilities and travel to other locations when needs arise
Complies with Avacare, Clinic, and Sponsor policies, standard operating procedures (SOPs) and guidelines
Performs other duties as assigned
Qualification
Required
Must demonstrate the ability to fulfill responsibilities of CRC Level I
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
Knowledge and experience of site operations and the drug development process
Excellent written and verbal communication skills – must be comfortable and effective in communicating with potential study participants from a diverse population
Interpersonal skills - open to others' ideas and willing to learn new things; respond well to questions and challenges
Process improvement – support ideas and theories on process improvement for efficiency and effectiveness
Computer proficiency in use of Microsoft Word, Excel
Benefits
Incentive plans
Bonuses
Health and welfare and/or other benefits
Company
IQVIA
IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
Founded in 1982
10001+ employees
Funding
Current Stage
Public CompanyTotal Funding
$3.5B2025-06-02Post Ipo Debt· $2B
2023-11-14Post Ipo Debt· $500M
2023-05-18Post Ipo Debt· $1B
Leadership Team
Chris Colapietro
Vice President, Customer Engagement
Jonathan Morris
VP & GM US Healthcare
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