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Senior 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: Approximately 5h per week Role: Clinical Specialist Start: immediate Contract based About IQVIA ...

ICON

Senior Clinical Research Associate

Atlanta, GA · On-site +1

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON is a global ... Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their ...

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 closeout * Serve as the primary contact for assigned clinical trials within your country * Ensure ...

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 closeout * Serve as the primary contact for assigned clinical trials within your country * Ensure ...

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 ...

Artivion

Sr. Clinical Data Manager

Kennesaw, GA

The Sr. Clinical Data Manager is responsible for data management operations and for the organization, coordination and execution of data management activities for assigned studies and projects. This ...

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Senior Clinical Trial Manager information

See Decatur, GA salary details

$21.5K

$122.3K

$201.1K

How much do senior clinical trial manager jobs pay per year?

As of Aug 21, 2026, the average yearly pay for senior clinical trial manager in Decatur, GA is $122,325.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $153,300.00 per year, depending on experience, location, and employer.

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

To thrive as a Senior Clinical Trial Manager, you need expertise in clinical trial operations, regulatory compliance, and project management, typically supported by a degree in life sciences or a related field and several years of clinical research experience. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications such as ACRP or SOCRA are often required. Exceptional leadership, problem-solving, and communication skills help manage teams, stakeholders, and complex timelines. These skills and qualities are critical to ensure trials are conducted efficiently, ethically, and in compliance with regulatory standards.

How does a senior clinical trial manager typically collaborate with cross-functional teams during a clinical study?

A Senior Clinical Trial Manager regularly works with cross-functional teams, including data management, regulatory affairs, biostatistics, and clinical operations, to ensure seamless execution of clinical studies. They facilitate communication between departments to address challenges, monitor study progress, and ensure compliance with protocols and regulatory requirements. This collaboration is essential for timely trial delivery and maintaining data integrity, as well as for problem-solving and decision-making throughout the study lifecycle.

What is the difference between Senior Clinical Trial Manager vs Clinical Trial Coordinator?

AspectSenior Clinical Trial ManagerClinical Trial Coordinator
ResponsibilitiesOversees entire trial process, manages teams, ensures complianceAssists with trial logistics, manages documentation, supports trial staff
Required CredentialsTypically requires a Bachelor's/Master's in life sciences, experience in trial managementUsually requires a Bachelor's in health sciences or related field
Work EnvironmentLeads trial teams, interacts with sponsors, regulatory bodiesSupports trial operations, coordinates between sites and teams
Industry UsageCommonly employed in pharmaceutical and biotech companiesOften found in clinical research sites and CROs

The main difference is that the Senior Clinical Trial Manager has a leadership role overseeing the entire trial process, while the Clinical Trial Coordinator provides operational support. The manager handles strategic planning and team management, whereas the coordinator focuses on day-to-day trial activities.

What does a senior clinical trial manager do?

A senior clinical trial manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with cross-functional teams, manage budgets and timelines, and ensure data quality and safety throughout the trial process. Strong project management skills and knowledge of Good Clinical Practice (GCP) are essential for this role.

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

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

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

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

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

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

Senior Clinical Trial Manager jobs near you
Infographic showing various Senior Clinical Trial Manager job openings in Decatur, GA as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 16% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $122,325 per year, or $58.8 per hour.

Clinical Trial Rater

IQVIA

Atlanta, GA • Remote

Part-time

Posted 4 days ago

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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