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Cra Assistant Jobs in Arizona (NOW HIRING)

ICON

Clinical Research Associate

Phoenix, AZ · On-site +1

Document site progress and escalate risks or issues to the clinical team * Assist in tracking site budgets and ensuring timely site payments (as applicable) * Collaborate with cross-functional ...

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Clinical Research Associate II

Phoenix, AZ · On-site

$91K - $114K/yr

Document site progress and escalate risks or issues to the clinical team * Assist in tracking site budgets and ensuring timely site payments (as applicable) * Collaborate with cross-functional ...

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Clinical Research Associate

Phoenix, AZ · On-site

Document site progress and escalate risks or issues to the clinical team * Assist in tracking site budgets and ensuring timely site payments (as applicable) * Collaborate with cross-functional ...

Tenet Health

Manager - Radiology

Tucson, AZ · On-site

Will identify, study, and assist in resolving problems relating to the department. Manages staff ... Certified Radiology Administrator(CRA) #LI-SB3 * Collaborates on the annual department operating ...

Carondelet St. Marys Hospital

Manager - Radiology

Tucson, AZ · On-site

$35.25 - $48/hr

Will identify, study, and assist in resolving problems relating to the department. Manages staff ... Certified Radiology Administrator(CRA) #LI-SB3 Organization Description St. Marys Hospital ...

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How much do cra assistant jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for cra assistant in Arizona is $32.79, according to ZipRecruiter salary data. Most workers in this role earn between $16.80 and $45.74 per hour, depending on experience, location, and employer.

What is a CRA Assistant?

A Clinical Research Associate (CRA) Assistant supports clinical trials by managing documents, coordinating meetings, and assisting with regulatory compliance. They help ensure studies follow protocols and regulatory requirements. CRA Assistants often handle administrative tasks, maintain trial records, and communicate with clinical sites. Their role is essential in supporting CRAs and ensuring the smooth operation of clinical research processes.

What are the main responsibilities of a CRA Assistant?

As a CRA Assistant, your primary responsibilities include supporting clinical research associates with administrative tasks such as organizing trial documentation, maintaining study files, scheduling site visits, and tracking regulatory submissions. You may also assist in preparing reports, following up with clinical sites, and ensuring data accuracy and proper documentation. The role often involves close collaboration with other team members, including project managers, study coordinators, and regulatory staff. This supportive position is critical for maintaining smooth trial operations and provides valuable hands-on experience for those interested in advancing within clinical research.

What are the key skills and qualifications needed to thrive in the CRA Assistant position, and why are they important?

To thrive as a CRA Assistant, you need a solid understanding of clinical research processes, attention to detail, and a background in life sciences or healthcare. Experience with electronic data capture (EDC) systems, Microsoft Office Suite, and knowledge of Good Clinical Practice (GCP) guidelines or certifications are often required. Excellent organizational skills, proactive communication, and the ability to manage multiple tasks make candidates stand out. These attributes are vital to support clinical research associates (CRAs), ensure regulatory compliance, and facilitate smooth clinical trial operations.

Is it hard to get a CRA assistant job?

Getting a CRA assistant job can be competitive, often requiring relevant education such as a degree in life sciences or related fields, along with strong organizational and communication skills. Prior experience or knowledge of clinical trial processes and familiarity with regulatory guidelines can improve chances of hiring. Entry-level positions may have less strict requirements, but overall, securing the role involves demonstrating attention to detail and understanding of clinical research environments.

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The most popular types of Cra jobs in Arizona are:

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For Cra Assistant jobs in Arizona, the most frequently searched job titles are:

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Cra Assistant jobs near you
Infographic showing various Cra Assistant job openings in Arizona as of August 2026, with employment types broken down into 2% As Needed, 76% Full Time, 18% Part Time, 2% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $68,211 per year, or $32.8 per hour.

Clinical Research Associate I (CRA I)

CND Life Sciences

Scottsdale, AZ • On-site

Full-time

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

Description
Position Summary
The Clinical Research Associate (CRA) is responsible for overseeing and monitoring clinical trials conducted at CND's Clinical Research Center site and investigator sites sponsored by CND or in collaboration with external partners. This role ensures that studies are executed in compliance with study protocols, Good Clinical Practice (GCP) R3 guidelines, budget constraints, and established milestone timelines. The CRA must have a strong understanding of clinical trial methodologies, regulatory requirements, and the ability to collaborate effectively with the investigators and internal and external cross-functional teams. The CRA consistently upholds the highest standards of professionalism.
Job Responsibilities
  • Regulatory Compliance: Ensure all clinical trials are conducted in adherence to the study protocol, ICH-GCP guidelines, relevant regulations and SOPs. Manage central IRB tasks for participating sites from start-up through close-out.
  • CND Site Subject Visits: Assist providers with subject recruitment, scheduling and conducting site visits at the internal CND site as needed. Responsibilities may include obtaining informed consent (ICF), assessing inclusion/exclusion criteria, recording vitals, and performing blood draws as backup to CND CRC.
  • Site Initiation: Conduct site initiation visits remotely or in person to assess site readiness, including regulatory start-up, facility reviews, annual bio-calibrations, supply storage, staff qualifications and training, study procedures and data entry management. Ensure all required site documents are collected and tracked in compliance with regulatory requirements and internal Standard Operating Procedures (SOPs). May also involve updating clinicaltrials.gov with site-specific information.
  • Study Monitoring: Perform regular site monitoring visits remotely (via eCRF) or in person (via site source documents) per study-specific monitoring plans and timelines. Oversee data entry, protocol adherence, query resolution, quality compliance, and patient safety reporting, escalating protocol deviations or subject safety concerns as needed. Assist in the development of study-specific monitoring plans.
  • Site Communication: Maintain proactive communication with site staff, responding to inquiries timely and escalating urgent matters as necessary.
  • Site Engagement and Subject Recruitment: Monitoring weekly site recruitment logs to verify subject eligibility and enrollment. Assist sites with IRB approvals for advertising and recruitment strategies. Support community patient advocacy outreach when needed.
  • Site Invoices: Review and approve site invoices based on completed EDC data entry and query resolution for all subject visits invoiced, including start-up and close-out visits.
  • Data Management: Oversee the collection, processing, and documentation of study data. Ensure data integrity through thorough data review and timely query resolution following study-specific monitoring plan milestones.
  • Safety Reporting: Oversee the reporting of adverse events and serious adverse events, ensuring compliance with regulatory requirements.
  • Site Close-Out: Conduct site close-out activities to ensure proper data lock, storage, and archiving study documents.
  • Trial Documentation: Maintain and manage all clinical trial documents, ensuring they remain current and compliant with regulatory standards.
  • Team Collaboration: Work closely with internal and external cross-functional teams and vendors to ensure clinical trials are executed efficiently, within budget and in alignment with study milestones.
  • Reporting: Provide regular updates and comprehensive reports to the Senior Director of Clinical Research and/or designated CR lead and other stakeholders on trial progress.
  • Quality Assurance and Compliance Participate in internal and external audits, addressing findings, and implement corrective and preventive actions as necessary.
  • Perform other duties as assigned.

Knowledge, Skills & Experience
  • Minimum of 5 years of clinical research experience as a Clinical Research Coordinator or at least 2 years of experience as a Clinical Research Associate.
  • Therapeutic experience in neurology is highly preferred.
  • Experience in Phase I, II or III of clinical trials; familiarity with NIH and other government-sponsored protocols a plus.
  • In-depth knowledge of ICH-GCP guidelines and relevant regulatory requirements for clinical trial conduct.
  • Strong proficiency in IT tools including the MS 365 suite, Electronic Data Capture (EDC) systems, Clinical Trial Management Systems (CTMS) and other applicable technologies.
  • Excellent written and verbal communication skills.
  • Strong multitasking skills, attention to detail, creative problem-solving, and the ability to maintain accurate records.
  • Demonstratedability to identify and resolve site-related challenges with strong negotiation skills.
  • Proven ability to work effectively in a team-based environment.
  • Willingness and ability to travel to clinical sites as needed.

Education, Certifications, and Licensures
  • Bachelor's of Science degree or related field required.
  • The Collaborative Institutional Training Initiative (CITI) Good Clinical Practice (GCP) certification, or its equivalent, or willing to complete within first month of hire.
  • International Air Transport Association (IATA) certification, if indicated

Other
  • Combination of seated and standing work to complete the core functions of the role
  • Sit and stand for long periods of time
  • Visual acuity and analytical skills
  • This job will be expected to work onsite at CND's Scottsdale, AZ headquarters 3-5 days/week

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