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Global Clinical Trial Manager Jobs in Decatur, GA

IQVIA

Clinical Trial Rater

Atlanta, GA · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... Clinical Specialist Start: immediate Contract based About IQVIA IQVIA is a global leader in ...

New

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68K - $232K/yr

Lead end-to-end country-level trial management , from study start-up through database lock and ... Partner with CRA's, Global Project Leads, and cross-functional teams to ensure successful study ...

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68K - $232K/yr

Lead end-to-end country-level trial management , from study start-up through database lock and ... Partner with CRA's, Global Project Leads, and cross-functional teams to ensure successful study ...

Icon plc

Senior CRA

Atlanta, GA · On-site

Sr CRA - Oncology - GA FL - Astellas ICON is a global healthcare intelligence and clinical research ... management, with proficiency in relevant clinical trial software and tools. * Excellent ...

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Global Clinical Trial Manager information

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$93

How much do global clinical trial manager jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for global clinical trial manager in Decatur, GA is $61.04, according to ZipRecruiter salary data. Most workers in this role earn between $49.52 and $68.75 per hour, depending on experience, location, and employer.

What is a global clinical trial manager?

A Global Clinical Trial Manager is a professional responsible for overseeing the planning, execution, and management of clinical trials conducted across multiple countries or regions. Their main role involves coordinating study timelines, budgets, regulatory compliance, and collaboration among diverse teams to ensure that clinical research is conducted efficiently and ethically. They also manage relationships with vendors, clinical research organizations, and investigators, while ensuring that all data is collected and reported in accordance with regulatory standards. This role is critical in bringing new medicines and therapies to market on a global scale.

How does a global clinical trial manager navigate the challenges of coordinating multi-country studies?

As a Global Clinical Trial Manager, one of the main challenges is ensuring consistent communication and regulatory compliance across multiple countries. This often involves working closely with regional teams, understanding diverse regulatory requirements, and managing timelines that account for different time zones and local practices. Successful managers leverage project management tools, conduct regular cross-functional meetings, and build strong relationships with international stakeholders to keep studies on track. Adaptability, cultural sensitivity, and attention to detail are essential for overcoming these challenges and ensuring the trial's success.

What are the key skills and qualifications needed to thrive as a global clinical trial manager, and why are they important?

To thrive as a Global Clinical Trial Manager, you need expertise in clinical research, regulatory compliance, project management, and often a degree in life sciences or a related field. Familiarity with tools like electronic data capture (EDC) systems, project management software, and knowledge of GCP and ICH guidelines are typically required, as well as relevant certifications such as PMP or ACRP. Outstanding leadership, cross-cultural communication, and problem-solving skills set top professionals apart in coordinating multinational teams and stakeholders. These skills are crucial for ensuring trials are executed efficiently, ethically, and in compliance with global standards.

How much do global clinical trial managers make?

Global clinical trial managers typically earn between $90,000 and $150,000 annually, depending on experience, location, and the size of the organization. Senior managers or those with specialized skills and certifications can earn higher salaries, often exceeding $160,000. Compensation may also include bonuses and benefits related to project scope and responsibilities.

How much does a global clinical trial manager earn?

A global clinical trial manager typically earns between $90,000 and $150,000 annually, depending on experience, location, and the size of the organization. Senior managers or those with specialized skills and certifications can earn higher salaries, often exceeding $160,000. Compensation may also include bonuses and benefits related to project scope and responsibilities.

What are popular job titles related to Global Clinical Trial Manager jobs in Decatur, GA?

For Global Clinical Trial Manager jobs in Decatur, GA, the most frequently searched job titles are:

What job categories do people searching Global Clinical Trial Manager jobs in Decatur, GA look for?

The top searched job categories for Global Clinical Trial Manager jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Global Clinical Trial Manager jobs?

Cities near Decatur, GA with the most Global Clinical Trial Manager job openings:

Global Clinical Trial Manager jobs near you

Clinical Trial Rater

IQVIA

Atlanta, GA • 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 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

    Pay

    Benefits

    Hours and flexibility

    Workplace

    Get the full story on Breakroom

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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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