Clinical Research Coordinator, On-Site, Salt Lake City, Utah at IQVIA

Salt Lake City, Utah, United States

IQVIA Logo
Not SpecifiedCompensation
Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Clinical Research, HealthcareIndustries

Requirements

  • Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens
  • Solid understanding of site operations and the drug development process
  • CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants
  • CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants
  • Strong written and verbal communication skills, with attention to detail and time management
  • Comfortable using CTMS, eCRFs, and Microsoft Office tools

Responsibilities

  • Manage 2–6 trials of varying complexity
  • Perform clinical procedures
  • Lead study coordination from start to finish
  • Handle patient recruitment and informed consent
  • Manage regulatory documentation and site audits
  • Work closely with investigators, sponsors, and monitors
  • Mentor junior staff and contribute to internal training

Skills

phlebotomy
vital signs
ECGs
lab specimens processing
patient recruitment
informed consent
regulatory documentation
site operations
study coordination
clinical procedures

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters
1998Year Founded
$3,526MTotal Funding
POST_IPO_EQUITYCompany Stage
Cybersecurity, Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.
Proliferation of disparate technological solutions causes technology overload in clinical trials.
Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.
The company offers privacy-enhancing technologies to protect individual patient data.
IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.
AI-driven drug discovery accelerates identification of potential drug candidates.
Expansion of telemedicine facilitates remote patient monitoring and data collection.

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