IQVIA · 15 hours ago
Research Assistant, On-Site, Pleasant View, UT
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. This role involves assisting in the conduct of clinical trial activities, developing relationships with study team members, and ensuring compliance with regulatory guidelines.
AnalyticsHealth CareLife Science
Responsibilities
Develop strong working relationships and maintain effective communication with study team members
Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office
Assist with the screening, recruiting and enrollment of research subjects
Perform patient/research participant scheduling
Collect patient/research participant history
Data entry and Management
Coordinate follow-up care and laboratory procedures
Adhere to an IRB approved protocol
Assist in the informed consent process of research subjects
Support the safety of research subjects
Coordinate protocol related research procedures, study visits, and follow-up care
Comply with organization, and Sponsor policies, standard operating procedures (SOPs) and guidelines
Schedule subject visits and procedures
Qualification
Required
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
Strong interpersonal skills with attention to detail a must
Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint) and with clinical trial master filing systems
Benefits
Incentive plans
Bonuses
Health and welfare
Company
IQVIA
IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
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
Recent News
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