IQVIA · 21 hours ago
Clinical Research Coordinator, On-Site, Kansas City, Missouri
Kansas City, MO
Full-time
Onsite
Entry, Mid Level
$37K/yr - $107K/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, managing patient recruitment, and supporting study team objectives.
AnalyticsHealth CareLife Science
Responsibilities
Ability to coordinate as primary CRC 1-3 studies on average of low to medium complexity, with oversight by a manager or higher-level CRC
May assist as back-up CRC on other studies
Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved
Obtains informed consent of research subjects
Develops strong working relationships and maintain effective communication with study team members
Completes all protocol related training
Performs patient/research participant scheduling
Collects patient/research participant 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
Supports the safety of research subjects, report adverse events
Coordinates protocol related research procedures, study visits, and follow-up
Facilitates pre-study, site qualification, study initiation, monitoring visits, and study close out activities
Collects, processes and ships laboratory specimens
May be asked to perform special project responsibilities and travel to other clinic locations, within the area, when needs arise
Complies with Avacare and Sponsor policies, standard operating procedures (SOPs) and guidelines
Performs other duties as assigned
Qualification
Required
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
Clinical Research Coordinator experience within a similar setting
Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc
Knowledge and experience of site operations and the drug development process
Effective communication
Computer proficiency in use of Microsoft Word, Excel
Benefits
Incentive plans
Bonuses
Other forms of compensation
A range of 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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