Clinical Research Coordinator, On-Site, Bountiful, Utah at IQVIA

Bountiful, Utah, United States

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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

Key technologies and capabilities for this role

phlebotomyECGsvital signslab specimens processingpatient recruitmentinformed consentregulatory documentationsite operationsstudy coordinationclinical procedures

Questions & Answers

Common questions about this position

Is this position remote or on-site?

This is a fully on-site position in Bountiful, Utah.

What clinical skills are required for this role?

Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens is required.

What experience is needed for the CRC I and CRC II positions?

CRC I requires a minimum of 1-3 years in a clinical research setting at a clinical investigative site working with participants, while CRC II requires a minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants.

What is the company culture like at Avacare?

Avacare offers a collaborative culture with a supportive team that values initiative, adaptability, and continuous learning.

What makes a strong candidate for this Clinical Research Coordinator role?

Strong candidates will have site operations knowledge, solid communication and documentation skills, attention to detail, time management, and technical proficiency with CTMS, eCRFs, and Microsoft Office tools.

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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