Clinical Trial Nurse - Gilbert, AZ at IQVIA

Gilbert, Arizona, United States

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Not SpecifiedCompensation

Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level

Part TimeJob Type

UnknownVisa

Healthcare, Clinical Research, PharmaceuticalsIndustries

Requirements

Knowledge of study protocols, source document forms, electronic data capture systems, Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) principles, sponsor SOPs, and relevant local guidelines/regulations
Ability to perform complex clinical research procedures including ECG, lab sample collection, spirometry, vital signs, dose verifications, cardiac telemetry monitoring, and questionnaire administration
Skills in lab testing, specimen collection preparation, and lab logistics
Up-to-date knowledge of current best nursing practices and clinical research topics
Ability to adhere to site policies, SOPs, FDA requirements, and clinical research regulations
Availability for part-time onsite support (8 hours/month) in Gilbert, AZ

Responsibilities

Provide clinical research support to investigators for preparing and executing studies
Review study protocols, source documents, and electronic data capture systems
Collect and submit regulatory/ethics documentation to FDA and other bodies
Recruit and screen patients, maintain screening/enrollment logs
Orient research subjects to study purpose, procedures, and requirements
Maintain source documentation per GCP/ICH principles
Schedule and execute study visits and delegated procedures under Principal Investigator supervision
Handle lab testing, specimen collection, and logistics
Monitor subject safety, report adverse events to Principal Investigator, team, and IRBs
Correspond with subjects to address study-related questions/concerns
Participate in meetings with site staff and Investigators to assign and execute tasks
Perform data quality checking and query resolution
Update and maintain site staff skills, training, and records
Assist investigators in safeguarding subject well-being and maintaining research standards
Maintain a safe environment and act as subject advocate
Address subject questions proactively and take remedial action
Advise site staff on nursing practices and study care delivery
Report deviations from research practices and implement changes
Verify study objectives are met on time, within budget, and per protocol/regulations
Provide training to new site staff on study-specific topics
Audit and maintain staff training records
Guide and supervise lower-level staff to follow protocols and SOPs
Participate in study process reviews, enhancements, budget control, and team development
Prepare for and attend monitoring visits, audits, and regulatory inspections
Assist with site staffing and scheduling coverage

Skills

Key technologies and capabilities for this role

GCPICHFDAECGpatient screeningpatient recruitmentsource documentationadverse event reportingstudy protocol reviewlab testingspecimen collectionIRBelectronic data capture

Questions & Answers

Common questions about this position

Is this position full-time or part-time?

This is a part-time position requiring 8 hours per month.

Is remote work allowed for this role?

No, the role requires onsite support.

What are the key responsibilities of the Clinical Trial Nurse?

Key responsibilities include coordinating clinical research studies, recruiting and screening patients, performing study procedures like ECG and lab sample collection, monitoring subject safety, and maintaining documentation per GCP and ICH principles.

What clinical skills are required for this position?

Required skills include performing ECG, lab sample collection, spirometry, vital signs measurement, dose verifications, cardiac telemetry monitoring, and questionnaire administration, along with knowledge of GCP/ICH principles.

What compensation or salary is offered for this role?

This information is not specified in the job description.

Where is this position located?

The position is located in Gilbert, AZ and requires onsite support.

What makes a strong candidate for this Clinical Trial Nurse role?

A strong candidate will have nursing experience in clinical research, proficiency in procedures like ECG, phlebotomy, and spirometry, familiarity with GCP/ICH guidelines, and skills in patient recruitment, safety monitoring, and regulatory documentation.

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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