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Clinical Trial Analyst Jobs (NOW HIRING)

IQVIA

Clinical Trial Rater

Chicago, IL · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... analytics, technology solutions, and clinical research services. We collaborate with top ...

IQVIA

Clinical Trial Rater

New Providence, NJ · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... analytics, technology solutions, and clinical research services. We collaborate with top ...

IQVIA

Clinical Trial Rater

Philadelphia, PA · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... analytics, technology solutions, and clinical research services. We collaborate with top ...

IQVIA

Clinical Trial Rater

Raleigh, NC · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... analytics, technology solutions, and clinical research services. We collaborate with top ...

IQVIA

Clinical Trial Rater

Washington, DC · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... analytics, technology solutions, and clinical research services. We collaborate with top ...

IQVIA

Clinical Trial Rater

Springfield, MA · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... analytics, technology solutions, and clinical research services. We collaborate with top ...

Prometrika LLC

Clinical Trial Associate II

Cambridge, MA · On-site

$75K - $90K/yr

The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research ... Analyze issues and use judgment to make decisions * Escalate non-standard problems or issues as may ...

Legend Biotech US

Senior Clinical Trial Associate

Somerset, NJ · Hybrid

$35.50 - $48.25/hr

Legend Biotech is seeking a Senior Clinical Trial Associate as part of the Clinical Operations team ... Detail-oriented with strong analytical and problem-solving skills. * Ability to work independently ...

ICON

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

As a Clinical Trial Liaison at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What you ...

410 ICR United States USA

$110K - $138K/yr

As a Clinical Trial Liaison at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What you ...

Icon plc

Clinical Trial Liaison

Blue Bell, PA

$110K - $138K/yr

As a Clinical Trial Liaison at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What you ...

Icon plc

Clinical Trial Liaison

Blue Bell, PA · On-site

$110K - $138K/yr

As a Clinical Trial Liaison at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What you ...

Biogen

Clinical Trial Manager

Cambridge, MA · On-site

$117K - $157K/yr

As a Clinical Trial Manager, you will be a vital part of the PO&T team within the Implantable ... analytical approach utilizing a combination of factors including, but not limited to, relevant ...

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Clinical Trial Analyst information

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How much do clinical trial analyst jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical trial analyst in the United States is $39.80, according to ZipRecruiter salary data. Most workers in this role earn between $31.49 and $45.67 per hour, depending on experience, location, and employer.

What does a clinical trial analyst do?

A Clinical Trial Analyst is responsible for managing and analyzing data collected during clinical trials to ensure accuracy and compliance with regulatory standards. They work closely with clinical research teams to monitor trial progress, identify trends, and help ensure that study protocols are being followed. Their work supports the evaluation of the safety and effectiveness of new drugs, treatments, or medical devices. Clinical Trial Analysts also assist with preparing reports and documentation for regulatory agencies and internal stakeholders.

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

To thrive as a Clinical Trial Analyst, you need a background in life sciences or related fields, strong analytical skills, and experience with clinical research protocols. Familiarity with data management systems, statistical software (such as SAS or SPSS), and regulatory compliance tools (e.g., FDA or ICH guidelines) is typically required. Attention to detail, effective communication, and problem-solving abilities help you collaborate with cross-functional teams and ensure data integrity. These skills are crucial for accurately analyzing trial data, maintaining compliance, and supporting the successful execution of clinical studies.

What are some common challenges faced by clinical trial analysts when managing multiple studies simultaneously?

Clinical Trial Analysts often juggle data from several studies at once, which can present challenges like managing competing deadlines, ensuring data accuracy, and maintaining clear communication with cross-functional teams. Prioritizing tasks and staying organized are essential for meeting regulatory timelines and preventing errors. Additionally, adapting quickly to protocol changes or unexpected issues is a key part of the role, as is collaborating with data managers, statisticians, and clinical operations teams to keep studies on track.

What is the difference between Clinical Trial Analyst vs Clinical Research Coordinator?

AspectClinical Trial AnalystClinical Research Coordinator
Required CredentialsBachelor's degree in life sciences, biostatistics, or related field; some roles may require certification in clinical researchBachelor's degree in health sciences, nursing, or related field; often requires certification in clinical research coordination
Work EnvironmentData analysis, report preparation, and monitoring clinical trial dataManaging trial logistics, patient recruitment, and site coordination
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, Clinical Trial Analysts focus on data analysis and reporting, whereas Clinical Research Coordinators handle trial logistics and patient management. Both positions require similar educational backgrounds and certifications, but their daily tasks and work environments differ significantly.

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Clinical Trial Analyst jobs near you
Infographic showing various Clinical Trial Analyst job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $82,791 per year, or $39.8 per hour.

Clinical Trial Rater

IQVIA

Chicago, IL • Remote

Part-time

Posted 21 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 Rater - Borderline Personality Disorder (BPD)

Location: Remote based in the US
Hours: Approximately 5h per week
Role: Clinical Specialist

Start: immediate

Contract based

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with top pharmaceutical and biotech companies to accelerate innovation and improve patient outcomes. Our mission is to combine data science and human expertise to transform healthcare worldwide.

We are seeking experienced and reliable Clinical Trial Raters to conduct standardized psychiatric assessments for a clinical trial in Borderline Personality Disorder (BPD). The rater will be responsible for administering validated clinicianrated instruments, ensuring high-quality, consistent data collection in accordance with the study protocol, GCP, and regulatory requirements.

This role requires strong clinical judgment, experience with psychiatric populations, and the ability to maintain objectivity and interrater reliability across multiple assessments and time points.

Key Responsibilities
  • Conduct structured and semistructured clinical interviews with trial participants diagnosed with Borderline Personality Disorder
  • Administer, score, and document validated psychiatric rating scales: CGI-S, and CGI-C or CGIC-S
  • Maintain interrater reliability, including participation in calibration, training, and quality review sessions
  • Identify and escalate safety concerns (e.g. suicidality) according to protocol and sponsor guidelines
  • Work closely with study investigators, site staff, and sponsor/CRO teams to support highquality trial execution
  • Adhere to Good Clinical Practice (GCP), SOPs, and ethical guidelines at all times
  • Maintain participant confidentiality and a traumainformed, empathetic approach during all assessments
    Required Qualifications
    • Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign Medical Doctor (FMD), or Doctor of Osteopathic Medicine (DO)
    • Licensure: Licensed Clinician:MD/FMD/DO, Psychiatrist, Clinical Psychologist,Psychotherapist, Mental Health Counselor/Practitioner(LMHC/LCMHC/LMHP)or Professional Counselor(LPC/LCPC/LPCC)
    • Clinical Experience: 3 years of clinical experience withBorderline Personality Disorder(BPD) population
    • Clinical Trial Rater Experience 3 years of experience as clinical trial rater, including semi-structured psychiatric assessments
    • 3 years of experience with Clinical Global Impression rating scales
      • Clinical Global Impression-Severity (CGI-S) and
      • Clinical Global Impression-Change (CGI-C) or
      • Clinical Global Impression-Change in Severity (CGIC-S)
    Why Work With Us?
    • Flexible, remote work schedule.
    • Opportunity to contribute to global clinical research.
    • Collaborate with a team committed to improving patient care and advancing science.

    #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 is 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

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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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