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Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

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

As of Aug 6, 2026, the average hourly pay for clinical trial assistant remote in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Trial Assistant Remote, you need a strong foundation in clinical research processes, attention to detail, and familiarity with regulatory compliance, often supported by a degree in life sciences or related field. Proficiency with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and knowledge of GCP (Good Clinical Practice) guidelines or related certifications is highly beneficial. Excellent organizational skills, proactive communication, and the ability to manage time effectively while working independently are key soft skills. These competencies are crucial for ensuring smooth trial operations, accurate documentation, and effective collaboration with clinical teams from a remote setting.

What is a clinical trial assistant remote?

A Clinical Trial Assistant (CTA) Remote job involves supporting clinical research teams in coordinating, documenting, and managing clinical trials from a remote location. Responsibilities typically include maintaining regulatory documents, tracking study progress, assisting with patient enrollment, and ensuring compliance with protocols and guidelines. CTAs work closely with Clinical Research Associates (CRAs) and Study Managers to facilitate smooth trial operations. Strong organizational skills, attention to detail, and proficiency with clinical trial management systems (CTMS) are essential for success in this role.

What does a clinical trial assistant remote do?

A typical day for a remote Clinical Trial Assistant involves managing and tracking important study documents, supporting site communications, ensuring data accuracy in trial management systems, and assisting with regulatory submissions. You’ll often coordinate with study coordinators, project managers, and other team members via email and virtual meetings to address queries and maintain trial timelines. The role requires a high level of organization and self-motivation, as you’ll balance multiple administrative tasks and respond quickly to shifting priorities. This collaborative and detail-oriented environment provides opportunities to expand your skills in clinical research and prepare for more advanced roles in the field.

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Clinical Trial Assistant Remote jobs near you
Infographic showing various Clinical Trial Assistant Remote job openings in the United States as of August 2026, with employment types broken down into 79% Full Time, 7% Part Time, and 14% Contract. Highlights an 100% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Job Posting Title Clinical Trial Psych Rater

IQVIA

Austin, TX • Remote

Part-time

Posted 13 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

60th of 221 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 BEHAVE,-AD, E-BEHAVE-AD, BEHAVE-AD-FW, NPIC, ADAS-Cog;CGI-S, C-SSRS)

    • 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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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

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