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Remote Clinical Trial Manager Jobs in Decatur, GA

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68.40K - $232.80K/yr

In this remote role you will serve as the primary country-level leader for clinical trial delivery ... Lead end-to-end country-level trial management , from study start-up through database lock and ...

New

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68.40K - $232.80K/yr

In this remote role you will serve as the primary country-level leader for clinical trial delivery ... Lead end-to-end country-level trial management , from study start-up through database lock and ...

New

CGI Inc.

Remote Clinical Nurse Auditor

Atlanta, GA · On-site +1

... management program. Note: This position is remote-friendly (anywhere in the U.S.), provided ... Clinical Validation: Document specified coding issues in conjunction with the DRG Validation Team ...

ICON

Senior Clinical Research Associate

Atlanta, GA · On-site +1

Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their reports. * Located in the US near a major airport. Ability to cover up to 65% regional travel.

IQVIA

TMF Quality Project Manager (Remote)

Atlanta, GA · Remote

$47.40K - $118.60K/yr

... regarding Trial Master Files. Apply clinical research records management expertise to provide ... This is a remote position open to candidates in the United States. IQVIA is a leading global ...

IQVIA

TMF Quality Project Manager (Remote)

Atlanta, GA · Remote

$47.40K - $118.60K/yr

... regarding Trial Master Files. Apply clinical research records management expertise to provide ... This is a remote position open to candidates in the United States. IQVIA is a leading global ...

Actalent

Remote Pharmacist

Atlanta, GA · Remote

$55/hr

Remote Clinical Pharmacist - Utilization Management We are seeking a dedicated Clinical Pharmacist to join our team in a fully remote capacity. You will be responsible for reviewing utilization ...

New

Actalent

Remote Pharmacist

Atlanta, GA · Remote

$55/hr

Remote Clinical Pharmacist - Utilization Management We are seeking a dedicated Clinical Pharmacist to join our team in a fully remote capacity. You will be responsible for reviewing utilization ...

New

Alimentiv

Consulting Statistician

Atlanta, GA · On-site +1

$110.50K - $184K/yr

Prepares statistical analysis plans and oversee project data collection, management, and analysis ... novel clinical trial designs and processes and statistical methodologies into publishable and ...

Alimentiv

Consulting Statistician

Atlanta, GA · Remote

Prepares statistical analysis plans and oversee project data collection, management, and analysis ... novel clinical trial designs and processes and statistical methodologies into publishable and ...

IQVIA

Lead Clinical Data Manager (Remote)

Atlanta, GA · Remote

$68.50K - $217.10K/yr

This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main ...

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$28

$61

$93

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

As of May 30, 2026, the average hourly pay for remote 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 Does a Remote Clinical Trial Manager Do?

Remote clinical trial managers monitor the process of clinical testing from home or another location outside of the office or lab. In this role, you may collaborate with the clinical project manager to create outlines for the trial, research relevant information from existing medical studies, and help ensure the scope of the testing is enough to move the product forward to the next phase. Products may include pharmaceuticals, medical devices, or other forms of medical treatments. Your job duties also involve creating strategies for efficient testing methods, checking that all tests comply with safety standards and current government regulations, documenting results, and supervising research assistants.

What are the key skills and qualifications needed to thrive as a Remote Clinical Trial Manager, and why are they important?

To thrive as a Remote Clinical Trial Manager, you need expertise in clinical research, regulatory compliance, and project management, usually supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and GCP certification are typically required. Exceptional organizational skills, proactive communication, and the ability to lead cross-functional teams remotely set top performers apart. These competencies are crucial for ensuring trial integrity, regulatory adherence, and seamless coordination across distributed teams.

How does a Remote Clinical Trial Manager typically collaborate with on-site study teams and stakeholders?

As a Remote Clinical Trial Manager, you will frequently coordinate with on-site study teams, investigators, and sponsors through virtual meetings, project management platforms, and regular reporting. Effective communication and proactive problem-solving are essential for ensuring trial milestones are met and regulatory requirements are followed, despite not being physically present. You may also oversee remote monitoring visits, address site queries, and facilitate cross-functional collaboration between data management, safety, and regulatory teams. This structure allows for flexibility while maintaining strong oversight and quality standards.

What is a Remote Clinical Trial Manager?

A Remote Clinical Trial Manager is a professional responsible for overseeing the planning, execution, and management of clinical trials from a remote location. They coordinate with various teams, ensure regulatory compliance, monitor trial progress, and manage budgets and timelines, all while working off-site. This role typically involves using digital tools to communicate, track data, and ensure the trial runs smoothly and efficiently. Remote Clinical Trial Managers are essential in facilitating clinical research, especially in decentralized or multi-site studies. They play a key role in ensuring that clinical trials meet both scientific and regulatory standards.

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

AspectRemote Clinical Trial ManagerRemote Clinical Research Associate
CredentialsTypically requires a Bachelor's or higher in life sciences, with experience in trial managementUsually holds a Bachelor's in life sciences or related field, with certification in clinical research (e.g., CCRP)
Work EnvironmentOversees multiple sites, manages trial timelines, budgets, and teams remotelyMonitors trial sites, ensures protocol compliance, and collects data remotely
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical research organizations

The Remote Clinical Trial Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Remote Clinical Research Associate primarily monitors trial sites and data collection. Both roles require clinical research knowledge and often work remotely within the same industry sectors.

More about Remote Clinical Trial Manager jobs
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Remote Clinical Trial Manager jobs near you
Clinical Project Lead, Oncology

Clinical Project Lead, Oncology

IQVIA

Atlanta, GA • Remote

$68.40K - $232.80K/yr

Full-time

Posted 2 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

54th of 203 rated it services

Job description

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 trial operations, drive performance, and collaborate cross-functionally to deliver high-quality data aligned with regulatory requirements and sponsor expectations.

This role is ideal for a clinical operations professional who thrives in a fast-paced, large matrixed environment and is passionate about improving patient outcomes through clinical research.

Key Responsibilities

Clinical Trial Delivery & Oversight

  • 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 delivery of high-quality, compliant data and documentation aligned with ICH-GCP, SOPs, and regulatory standards
  • Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target

Site & Stakeholder Management

  • Partner with CRA's, Global Project Leads, and cross-functional teams to ensure successful study execution
  • Lead site feasibility, selection, and activation processes
  • Drive investigator engagement and site performance, including recruitment and retention strategies

Operational Excellence & Compliance

  • Monitor study progress through systems and reports; implement corrective and preventive actions (CAPA) when needed
  • Ensure inspection readiness through complete and accurate trial documentation (CTMS, eTMF)
  • Oversee patient safety reporting (AEs/SAEs) within required timelines

Financial & Vendor Management

  • Manage country-level budgets, forecasting, and financial tracking
  • Oversee local vendors and site payments, ensuring timely and accurate processing

Regulatory & Quality Assurance

  • Coordinate ethics and regulatory submissions/approvals in collaboration with start-up teams
  • Ensure compliance with local regulations and global standards (ICH-GCP)

What You Bring

Required Qualifications

  • Bachelor's degree in life sciences, healthcare, or related field
  • Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
  • Excellent communication and stakeholder management skills
  • Proficiency in clinical systems (e.g., CTMS, eTMF)
  • 3-5+ years of total trial management experience
  • Experience managing complex or early-phase trials
  • Demonstrated ability to lead cross-functional teams and drive performance

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, when annualized, is $68,400.00 - $232,800.00. 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

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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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