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Remote Clinical Trial Transparency Jobs in Georgia

IQVIA

Clinical Trial Rater

Atlanta, GA · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

YO AI Labs

Clinicia Expert - Remote

Atlanta, GA · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess ...

YO AI Labs

Biostatistician Expert - Remote

Atlanta, GA · Remote

$60 - $70/hr

Remote Job Type: Contractor Pay: $60-$65/hour Job Overview We are looking for an experienced ... Analyze and validate clinical trial data. * Review and interpret Statistical Analysis Plans (SAPs)

YO AI Labs

Hematology Expert - Remote

Atlanta, GA · Remote

$150 - $200/hr

Hematology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess ...

YO AI Labs

Oncology Expert - Remote

Atlanta, GA · Remote

$150 - $200/hr

Oncology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess ...

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68K - $232K/yr

In this remote role you will serve as the primary country-level leader for clinical trial delivery , ensuring studies are executed efficiently from start-up through closeout. You will oversee local ...

Danaher

Principal Clinical Scientist

Atlanta, GA · On-site +1

This role is responsible for clinical trial strategies within the US and EU regions for Danaher ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

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Remote Clinical Trial Transparency information

What is a remote clinical trial transparency professional?

A Remote Clinical Trial Transparency professional is responsible for ensuring that information about clinical trials is accurately disclosed and made accessible to the public, regulators, and other stakeholders while working remotely. Their work involves preparing, reviewing, and submitting clinical trial data, maintaining compliance with global regulations, and protecting patient confidentiality. They ensure transparency by posting trial results to public registries, responding to disclosure requests, and supporting ethical standards in clinical research.

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

To thrive as a Remote Clinical Trial Transparency Specialist, you need a solid understanding of clinical research processes, regulatory requirements (like FDA, EMA, or ICMJE), and often a degree in life sciences or healthcare. Familiarity with trial disclosure platforms (such as ClinicalTrials.gov and EudraCT), document management systems, and data anonymization tools is typically required. Strong attention to detail, analytical thinking, and effective written communication are crucial soft skills for ensuring accuracy and compliance. These abilities are vital to uphold regulatory standards, protect patient privacy, and promote trust through transparent clinical trial reporting.

What are some common challenges faced by professionals in a remote clinical trial transparency role, and how can they be addressed?

Professionals in Remote Clinical Trial Transparency roles often encounter challenges such as managing large volumes of sensitive data, ensuring regulatory compliance across multiple jurisdictions, and coordinating with global stakeholders virtually. Effective organization, strong communication skills, and staying up to date with evolving regulations are key to addressing these challenges. Utilizing secure data management platforms and fostering clear communication channels with cross-functional teams can help ensure both transparency and compliance in a remote environment.

What is the difference between Remote Clinical Trial Transparency vs Remote Clinical Data Manager?

AspectRemote Clinical Trial TransparencyRemote Clinical Data Manager
Primary FocusEnsuring transparency of clinical trial results and compliance with reporting regulationsManaging and cleaning clinical trial data for analysis and reporting
Required CredentialsRegulatory knowledge, clinical trial experience, often a degree in life sciencesBiostatistics, data management certifications, degree in health sciences or related field
Work EnvironmentRemote, regulatory agencies, pharmaceutical companies, CROsRemote, pharmaceutical companies, CROs, data management teams

While both roles operate remotely within the clinical research industry, Remote Clinical Trial Transparency focuses on reporting compliance and transparency of trial results, whereas Remote Clinical Data Managers handle the technical aspects of data collection and management. Both require knowledge of clinical processes but serve different functions in the clinical trial lifecycle.

What are the most commonly searched types of Clinical Trial Transparency jobs in Georgia?

The most popular types of Clinical Trial Transparency jobs in Georgia are:

What are popular job titles related to Remote Clinical Trial Transparency jobs in Georgia?

For Remote Clinical Trial Transparency jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Trial Transparency jobs in Georgia look for?

The top searched job categories for Remote Clinical Trial Transparency jobs in Georgia are:

What cities in Georgia are hiring for Remote Clinical Trial Transparency jobs?

Cities in Georgia with the most Remote Clinical Trial Transparency job openings:

Remote Clinical Trial Transparency jobs near you
Infographic showing various Remote Clinical Trial Transparency job openings in Georgia as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 100% Remote job distribution.

Clinical Trial Rater

Atlanta, GA • Remote

IQVIA
Health Care and Social Assistance • 10K+ employees

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 225 rated it services

People enjoy working here

Good employer

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Learn more about IQVIAexternal

Part-time

Posted 9 days ago

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.
    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

    View All IQVIA Jobs

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