1

Decentralized Clinical Trials Jobs (NOW HIRING)

As a Principal Clinical System Lead, working as a Decentralized Clinical Trials Lead exclusively assigned and embedded within a Pharmaceutical Company, you will provide strategic leadership and ...

This role requires deep expertise in clinical trial operations, decentralized clinical trials, vendor oversight, and operational execution within regulated healthcare environments. As both a ...

Clinical Trial Coordinator

Miami, FL · On-site

$55K - $70K/yr

Requirements Required • 2 to 4 years of experience in clinical trials, patient recruitment, pharmacy operations, or decentralized clinical programs. • Strong interpersonal and training skills ...

Clinical Trial Coordinator

Orlando, FL · On-site

$55K - $70K/yr

Requirements Required • 2 to 4 years of experience in clinical trials, patient recruitment, pharmacy operations, or decentralized clinical programs. • Strong interpersonal and training skills ...

Clinical Trial Coordinator

Miami, FL · On-site

$55K - $70K/yr

Requirements Required • 2 to 4 years of experience in clinical trials, patient recruitment, pharmacy operations, or decentralized clinical programs. • Strong interpersonal and training skills ...

... clinical trials, healthcare settings, and everyday life. Our digital cognitive assessments are ... efficiencies, decentralized methodologies, partner integrations and self-service models. The ...

Significant experience in clinical research, decentralized clinical trials, clinical operations, project management, patient/site services, or related healthcare services. * Experience supporting ...

next page

Showing results 1-20

Decentralized Clinical Trials information

See salary details

$28

$62

$96

How much do decentralized clinical trials jobs pay per hour?

As of Jul 29, 2026, the average hourly pay for decentralized clinical trials in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

How much money can I make doing clinical trials?

Decentralized clinical trial coordinators and staff typically earn between $40,000 and $80,000 annually, depending on experience, location, and responsibilities. Compensation can include hourly wages, stipends, or per-study payments, especially for part-time or contract roles. Skills in data management and regulatory compliance can influence earning potential.

Is CRC an entry level position?

A Clinical Research Coordinator (CRC) position in decentralized clinical trials is often considered entry level, suitable for individuals with a bachelor's degree in a related field and strong organizational skills. However, some roles may require prior experience or certifications such as GCP training, depending on the complexity of the trial. Entry requirements vary by organization and trial phase.

How does working in Decentralized Clinical Trials differ from traditional clinical research roles in terms of daily collaboration and responsibilities?

In a Decentralized Clinical Trials (DCT) role, professionals often collaborate remotely with cross-functional teams, including investigators, data managers, and technology vendors, to manage trial activities. Unlike traditional site-based roles, much of the patient monitoring, data collection, and communication are conducted virtually, requiring adaptability to digital platforms and strong organizational skills. Daily responsibilities may include troubleshooting technical issues with remote monitoring devices, ensuring data quality from diverse sources, and coordinating with participants and team members across various locations. This environment fosters a dynamic, tech-driven workflow and often offers greater flexibility, but also demands proactive communication and problem-solving to address challenges that arise from decentralized operations.

Which clinical trials pay the most money?

Decentralized clinical trial roles that involve senior positions, project management, or specialized skills such as data analysis and regulatory expertise tend to offer higher compensation. Additionally, roles requiring extensive experience or certifications in clinical research often pay more, especially in leadership or oversight positions within the trial process.

What are decentralized clinical trials?

Decentralized clinical trials (DCTs) are studies that use digital technology and remote methods to conduct research outside traditional clinical sites. Instead of requiring participants to travel to a central location, DCTs enable data collection through telehealth, wearable devices, home visits, and mobile apps. This approach can increase participant convenience, improve access to diverse populations, and reduce costs. DCTs are becoming increasingly popular as they leverage technology to make clinical research more flexible and patient-centered.

What is the difference between Decentralized Clinical Trials vs Clinical Research Coordinators?

AspectDecentralized Clinical TrialsClinical Research Coordinators
CredentialsOften require clinical research experience, certifications like CCRP or CCRCTypically hold a bachelor's degree in health or related fields, with certifications like CCRP beneficial
Work EnvironmentConducted across multiple locations, including patients' homes and digital platformsWork primarily in clinical settings, hospitals, or research sites
Industry UsageUsed in innovative, patient-centric trial designsStandard role in traditional clinical trial settings

Decentralized Clinical Trials focus on remote, flexible patient engagement using digital tools, while Clinical Research Coordinators manage traditional, site-based trials. Both roles require clinical research knowledge but differ in work environment and trial approach.

Who decentralized clinical trials?

Decentralized clinical trials are conducted by professionals such as clinical research coordinators, trial managers, and data analysts who utilize digital tools, telemedicine, and remote monitoring technologies to facilitate patient participation outside traditional clinical settings. These roles require knowledge of regulatory requirements, good clinical practice, and often involve remote communication skills.

What are the key skills and qualifications needed to thrive in Decentralized Clinical Trials, and why are they important?

To thrive in Decentralized Clinical Trials, you need a solid background in clinical research, regulatory compliance, and data management, often supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, remote monitoring technologies, and platforms for virtual patient engagement is crucial. Strong organizational skills, adaptability, and clear communication help professionals manage remote teams and ensure participant retention. These skills and tools are essential for maintaining data integrity, regulatory adherence, and efficient trial operations in a decentralized environment.
More about Decentralized Clinical Trials jobs
What cities are hiring for Decentralized Clinical Trials jobs? Cities with the most Decentralized Clinical Trials job openings:
What are the most commonly searched types of Decentralized Clinical Trials jobs? The most popular types of Decentralized Clinical Trials jobs are:
What states have the most Decentralized Clinical Trials jobs? States with the most job openings for Decentralized Clinical Trials jobs include:
Infographic showing various Decentralized Clinical Trials job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Decentralized Clinical Trials Lead

410 ICR United States USA

Blue Bell, PA • On-site

Full-time

Posted yesterday


Job description

DCT Lead

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Principal Clinical System Lead, working as a Decentralized Clinical Trials Lead exclusively assigned and embedded within a Pharmaceutical Company, you will provide strategic leadership and direction in the design, development, and implementation of eCOA (electronic Clinical Outcome Assessment) clinical systems and technologies.

What You Will Do:

You will support the Sponsor’s eCOA clinical systems, taking a leadership role in eCOA project implementation, ensuring that deliverables meet quality, cost and timeline expectations.
Key responsibilities include:

• Lead study-specific eCOA technology deployment and management strategies for internal stakeholders and externally across functions and service providers

• Participate and collaborate with key process partners (e.g. Clinical Supplies, Biostatistics, Vendor Management, Procurement) in the sourcing, evaluation and audit/qualification of eCOA vendors

• Act as the sponsor eCOA SME and project manager for study deployment projects

• Lead study teams in development of study-specific user requirements specifications documents and user acceptance testing (UAT) protocols and execution. Ensure Good Documentation Practices are followed

• Provide support to study teams to resolve eCOA issues during the conduct of the study

• Collaborate with study teams during the protocol development process to understand requirements for eCOA technologies

• Effectively manage operational delivery with eCOA service providers; collect issues and trends from study teams; proactively work with Vendor Management and eCOA vendors for issue resolution and prevention

• Collaborate internally and with eCOA service providers to implement standards on both system design and data reporting

• Ensure the availability and delivery of training programs for relevant internal staff

• Collaborate with and supports other teams by streamlining data flow between eCOA and other systems (e.g. CTMS, Data Warehouse, Clinical Gateway, Clinical Supplies Management System)

• Ensure trust through transparency in communication and individual actions; ensure outcomes are organizationally driven rather than individually driven; promote collaborative organizational success

• Develop strategies to prioritize and deliver eCOA related initiatives in coordination with multiple internal departments

• Direct activities of eCOA vendors, ensuring compliance with specifications and the oversight of timelines and budgets

• Coordinate evaluation and impact assessment of changes in the eCOA landscape and makes recommendations for actions

• Provide support to teams on audit-related issues for eCOA services

• Ensure audit and inspection observations are evaluated and remediated in conjunction with the study team

Your Profile:


Required qualifications and experience:

  • Bachelor's degree in computer science, information technology, or a related discipline
  • 8+ years of relevant experience in a Clinical Research technology-related role within the Pharmaceutical, CRO, or technology vendor industries
  • Strong knowledge / experience with eCOA/ePRO systems and their function within clinical trials
  • Experience with eConsent/Telehealth/Connected Solutions is preferred for this position
  • Proven leadership skills with the ability to effectively manage cross-functional teams and projects
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with internal and external stakeholders
  • Detail-oriented with strong analytical and problem-solving abilities
  • Experience with technology evaluation, deployment, and project management
  • Willingness to travel as required (approximately 15%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply