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Clinical Trial Associate Part Time Jobs in Arizona

Clinical Trial Psych Rater - US Spanish Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Clinical Trial Psych Rater

Mesa, AZ · Remote

$62K - $156K/yr

Clinical Trial Psych Rater - US Spanish Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Clinical Trial Psych Rater

Gilbert, AZ · Remote

$62K - $156K/yr

Clinical Trial Psych Rater - US Spanish Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Part-Time Optician (Research)

Chandler, AZ · On-site

$17 - $21.75/hr

DR Part-time positions available We're looking for an experienced and detail-oriented Optician to ... You'll work closely with our study coordinators and investigators to perform key clinical trial ...

Part-Time Optician (Research)

Chandler, AZ · On-site

$17 - $21.75/hr

DR Part-time positions available We're looking for an experienced and detail-oriented Optician to ... You'll work closely with our study coordinators and investigators to perform key clinical trial ...

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Showing results 1-20

Clinical Trial Associate Part Time information

See Arizona salary details

$16

$37

$65

How much do clinical trial associate part time jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for clinical trial associate part time in Arizona is $37.26, according to ZipRecruiter salary data. Most workers in this role earn between $30.00 and $41.01 per hour, depending on experience, location, and employer.

What does a clinical trial associate part time do?

A Clinical Trial Associate (CTA) Part Time supports the administrative aspects of clinical research studies on a reduced schedule. Their responsibilities include organizing trial documentation, assisting with regulatory submissions, maintaining study files, and coordinating communication between research teams and clinical sites. Part-time CTAs may work in hospitals, research organizations, or pharmaceutical companies, helping ensure that trials comply with protocols and regulatory requirements. This role is ideal for individuals seeking flexible work arrangements while contributing to important medical research.

What are some typical responsibilities of a part-time clinical trial associate, and how do they balance workload with limited hours?

Part-time Clinical Trial Associates often handle essential tasks such as managing trial documentation, assisting with regulatory submissions, and supporting study coordinators. Balancing workload with limited hours requires strong organizational skills and effective communication with the team to prioritize tasks and ensure timely completion. They may also attend meetings, help maintain trial databases, and coordinate with investigators and site staff. Many organizations support flexible scheduling and clear task delegation to help part-time associates integrate seamlessly while meeting project deadlines.

What are the key skills and qualifications needed to thrive as a clinical trial associate part time, and why are they important?

To thrive as a Clinical Trial Associate Part Time, you need a strong understanding of clinical research processes, regulatory compliance, and attention to detail, often supported by a life sciences degree or relevant experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Excellent organizational skills, proactive communication, and teamwork are crucial soft skills for managing study documentation and supporting trial operations. These competencies ensure accurate trial execution, regulatory adherence, and smooth coordination within clinical research teams.

What is the difference between Clinical Trial Associate Part Time vs Clinical Trial Coordinator?

AspectClinical Trial Associate Part TimeClinical Trial Coordinator
CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, experience in clinical research
Work EnvironmentPart-time, office and clinical sitesFull-time, primarily office-based with site visits
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch institutions, hospitals, pharmaceutical companies
Common Search & ComparisonYesYes

The main difference between a Clinical Trial Associate Part Time and a Clinical Trial Coordinator lies in their work hours and scope. The part-time associate typically works fewer hours and focuses on specific trial tasks, while the coordinator manages broader trial activities full-time. Both roles require similar educational backgrounds and are integral to clinical research teams.

What are popular job titles related to Clinical Trial Associate Part Time jobs in Arizona?

For Clinical Trial Associate Part Time jobs in Arizona, the most frequently searched job titles are:

What cities in Arizona are hiring for Clinical Trial Associate Part Time jobs?

Cities in Arizona with the most Clinical Trial Associate Part Time job openings:

Infographic showing various Clinical Trial Associate Part Time job openings in Arizona as of August 2026, with employment types broken down into 2% As Needed, 76% Full Time, 15% Part Time, and 7% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $77,504 per year, or $37.3 per hour.

Clinical Trial Psych Rater

IQVIA

Glendale, AZ • Remote

$62K - $156K/yr

Part-time

Posted 17 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

63rd of 226 rated it services


Job description

Clinical Trial Psych Rater - US Spanish Speaking

Location: Remote/Virtual
Hours: Estimated 10-16 hours per month
Role: Clinical Specialist

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.

Position Overview

The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation.

Key Responsibilities

  • Participate in all required orientation, training, and calibration activities.

  • Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available.

  • Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring.

  • Complete assigned tasks and rater interactions according to schedule.

  • Submit all required documentation accurately and on time.

Required Qualifications

  • Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.

  • Experience:

    • Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically PANSS, MINI and CGI-SCH).

    • Minimum 3 years of clinical experience with psychiatric populations.

    • Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research).

    • Experience in CNS trials preferred.

  • Skills:

    • Strong interpersonal and communication skills for professional interaction at all levels.

    • Excellent organizational skills, attention to detail, time management, and problem-solving ability.

    • Proficiency with Windows and Microsoft Office applications.

Language Requirement

Current openings require fluency in English and native-level proficiency in US Spanish.

#LI-DNP #LI-Remote #LI-HCPN

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $62,700.00 - $156,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


IQVIA logo

About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US