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Remote Clinical Trial Consulting Jobs (NOW HIRING)

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

New

This is a remote position. This role offers the opportunity to support the planning and execution ... Support the day-to-day coordination of clinical trials. * Maintain and organize Trial Master File ...

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

New

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

New

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

Senior Clinical Trial Manager

Blue Bell, PA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Trial Manager, Biotech - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Global Clinical Trial Leader

South San Francisco, CA · Remote

$80 - $89.58/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Job Title: Global Clinical Trial Leader Location: South San Francisco, CA Type: Contract ... Hybrid - onsite and remote Hours: Monday through Friday - Standard eight (8 AM to 4 PM or 9 AM to 5 ...

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Remote Clinical Trial Consulting information

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$70

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

As of Aug 15, 2026, the average hourly pay for remote clinical trial consulting in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What is remote clinical trial consulting?

Remote clinical trial consulting involves providing expert guidance and support for clinical trials from a remote location, rather than on-site. Consultants in this field help pharmaceutical companies, research organizations, and healthcare providers design, manage, and monitor clinical trials. Their responsibilities may include protocol development, regulatory compliance, study management, data analysis, and ensuring ethical conduct. By working remotely, consultants can collaborate with global teams, leverage digital tools, and offer flexible, cost-effective solutions for clinical research projects.

What is the difference between Remote Clinical Trial Consulting vs Remote Clinical Research Associate?

AspectRemote Clinical Trial ConsultingRemote Clinical Research Associate
CredentialsTypically requires advanced degrees (e.g., MS, PhD), industry certifications (e.g., CCRP)Usually requires a bachelor's or master's in life sciences, with some certifications (e.g., CCRP)
Work EnvironmentConsultants work remotely, providing strategic advice to sponsors or CROsRemote monitoring and site management, often working directly with trial sites
Employer & Industry UsageConsulting firms, pharmaceutical companies, CROsPharmaceutical companies, CROs, biotech firms

Remote Clinical Trial Consulting involves providing strategic, regulatory, and operational advice remotely, often to sponsors or CROs. In contrast, Remote Clinical Research Associates focus on site monitoring, data collection, and trial oversight, typically working directly with trial sites. Both roles require industry knowledge but differ in responsibilities and work scope.

What are some common challenges faced by remote clinical trial consultants, and how can they be overcome?

Remote clinical trial consultants often encounter challenges such as coordinating across multiple time zones, maintaining clear communication with on-site teams, and ensuring data integrity when working virtually. To address these, consultants should leverage robust project management and communication tools, establish regular check-ins with stakeholders, and follow strict data security protocols. Building strong relationships with site staff and fostering a proactive approach to problem-solving also help ensure trial objectives are met efficiently despite the remote setup.

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

To excel as a Remote Clinical Trial Consultant, you need expertise in clinical research protocols, regulatory compliance, and data analysis, typically supported by a degree in life sciences or a related field and experience in clinical trials. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like GCP (Good Clinical Practice) are highly valued. Strong communication, problem-solving, and organizational abilities are essential for collaborating with diverse teams and managing projects remotely. These skills and qualifications ensure trials run efficiently, adhere to regulatory standards, and produce reliable, high-quality results.
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What cities are hiring for Remote Clinical Trial Consulting jobs?

Cities with the most Remote Clinical Trial Consulting job openings:

What are the most commonly searched types of Clinical Trial Consulting jobs?

The most popular types of Clinical Trial Consulting jobs are:

What states have the most Remote Clinical Trial Consulting jobs?

States with the most job openings for Remote Clinical Trial Consulting jobs include:

Infographic showing various Remote Clinical Trial Consulting job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Clinical Trial Psych Rater

IQVIA

Danvers, MA • Remote

Part-time

Posted 3 days ago

New


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services


Job description

Clinical Trial Psych Rater - Hungarian 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 SCID-5; PANSS; CGI)

    • 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 Hungarian.

#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