IQVIA · 1 day ago
Clinical Research Coordinator, On-Site, Kenner, Louisiana
New Orleans, LA
Full-time
Onsite
New Grad, Entry Level
$0/yr - $0/yrIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. They are seeking a Clinical Research Coordinator to coordinate and participate in clinical research studies, ensuring compliance with protocols and regulations while actively recruiting participants and managing study-related tasks.
AnalyticsHealth CareLife Science
Responsibilities
Coordinate clinical research studies conducted by a supervising principle investigator
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
Effective communication
Computer proficiency in use of Microsoft Word, Excel
Preferred
Clinical Research Coordinator experience within a similar setting preferred
Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc
Knowledge and experience of site operations and the drug development process
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
H1B Sponsorship
IQVIA has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (167)
2024 (294)
2023 (261)
2022 (229)
2021 (208)
2020 (180)
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
Recent News
Sabin Vaccine Institute
2025-12-04
Company data provided by crunchbase