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Contract Clinical Trial Assistant Jobs in Riverside, CA

Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...

Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...

Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...

Clinical Trial Agreements * Research Finance * Healthcare Administration * Grants Administration Hard Skills * Budget Development * Financial Analysis * Contract Negotiation * Cost Analysis * Trial ...

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

Clinical Trial Administration * Assist with trial start-up, including preparing and submitting regulatory and ethics documents, such as IRB/EC submissions, contracts, and site feasibility ...

Clinical Research Associate

Irvine, CA · On-site

$120K - $135K/yr

Clinical Trial Administration * Assist with trial start-up, including preparing and submitting regulatory and ethics documents, such as IRB/EC submissions, contracts, and site feasibility ...

Coordinate clinical trial device procurement, shipments, tracking, and returns. * Maintain TMF and clinical study documentation . * Monitor study inventory and assist with forecasting. * Track device ...

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Contract Clinical Trial Assistant information

See Riverside, CA salary details

$12

$39

$71

How much do contract clinical trial assistant jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for contract clinical trial assistant in Riverside, CA is $39.30, according to ZipRecruiter salary data. Most workers in this role earn between $26.83 and $50.14 per hour, depending on experience, location, and employer.

What is a contract clinical trial assistant?

A Contract Clinical Trial Assistant (CTA) is a professional who provides administrative support to clinical research teams on a contractual basis. They help manage documents, organize trial-related materials, coordinate meetings, and ensure compliance with regulatory requirements. CTAs play a vital role in maintaining the accuracy and integrity of clinical trial data and often act as a liaison between different stakeholders. Contract CTAs are typically hired for specific projects or time periods, offering flexibility to both employers and employees.

What are the key skills and qualifications needed to thrive as a contract clinical trial assistant?

To thrive as a Contract Clinical Trial Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or a related field, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic trial master files (eTMF), and Good Clinical Practice (GCP) guidelines is typically required. Excellent communication, time management, and problem-solving abilities help you collaborate effectively with cross-functional teams and manage multiple priorities. These skills and qualifications ensure accurate documentation, regulatory compliance, and efficient trial support in a fast-paced clinical research environment.

What are some common challenges faced by contract clinical trial assistants, and how can they be managed effectively?

Contract Clinical Trial Assistants often juggle multiple studies and tight timelines, which can make prioritizing tasks and maintaining accuracy challenging. Effective organization, clear communication with study teams, and proactive follow-up on outstanding documents are essential for success. Since contract positions may involve working with various sponsors or CROs, adaptability and quick learning of new protocols and systems are also important. Building strong relationships with colleagues and staying updated on regulatory requirements can help manage these challenges and contribute to smooth trial operations.

What is the difference between Contract Clinical Trial Assistant vs Clinical Trial Assistant?

AspectContract Clinical Trial AssistantClinical Trial Assistant
CredentialsTypically requires a relevant degree or certification in life sciences or healthcareSame as Contract CTA, often requiring similar qualifications
Work EnvironmentContract-based, often temporary assignments at pharmaceutical or biotech companiesPermanent or temporary roles within clinical research organizations or sponsors
Employer & Industry UsageUsed by CROs, pharma companies for project-specific needsCommon in clinical research settings, both permanent and contract roles
Search & Comparison IntentOften searched for contract roles, project-based workBroader search for clinical trial support roles

The main difference between a Contract Clinical Trial Assistant and a Clinical Trial Assistant lies in employment type and duration. Contract CTAs work on temporary, project-specific assignments, while Clinical Trial Assistants may hold permanent or longer-term positions. Both roles require similar qualifications and are integral to clinical research teams.

What are popular job titles related to Contract Clinical Trial Assistant jobs in Riverside, CA?

For Contract Clinical Trial Assistant jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Contract Clinical Trial Assistant jobs in Riverside, CA look for?

The top searched job categories for Contract Clinical Trial Assistant jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Contract Clinical Trial Assistant jobs?

Cities near Riverside, CA with the most Contract Clinical Trial Assistant job openings:

Clinical Trial Psych Rater

IQVIA

Colton, CA • Remote

Part-time

Re-posted 12 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 rated it services


Job description

Clinical Trial Psych Rater - German 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 MINI; MADRS; CAPS; PCL-5; CSSRS; CGI: OR MINI; PANSS; AIMS; BARS; LSAS; PGI-S)

    • 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 German.

#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 at https://jobs.iqvia.com

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.


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Hours and flexibility

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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