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Clinical Trial Software Jobs in Raleigh, NC (NOW HIRING)

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Senior Clinical Research Associate

Raleigh, NC · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...

Icon plc

Senior Clinical Research Associate

Raleigh, NC · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...

Icon plc

Senior CRA

Cary, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...

410 ICR United States USA

Senior CRA

Raleigh, NC

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...

410 ICR United States USA

Senior CRA

Cary, NC

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...

IQVIA

Clinical Lead- CVRM

Durham, NC · On-site

Job Overview Clinical Leads are an integral part of clinical trial delivery, working alongside ... IT skills - Good software and computer skills, including Microsoft Office applications including ...

IQVIA

Clinical Lead- CVRM

Durham, NC

Job Overview Clinical Leads are an integral part of clinical trial delivery, working alongside ... IT skills - Good software and computer skills, including Microsoft Office applications including ...

IQVIA, Inc.

Clinical Lead- CVRM

Durham, NC · On-site

Job Overview Clinical Leads are an integral part of clinical trial delivery, working alongside ... Good software and computer skills, including Microsoft Office applications including but not ...

CTI

Study Activation Manager

Raleigh, NC · On-site

  • Medical

  • PTO

Proficiency with clinical trial management systems, start-up tracking tools, and standard business software systems. * Bachelor's degree in a scientific, health care, or related discipline, or ...

CTI

Study Activation Manager

Raleigh, NC · On-site

  • Medical

  • PTO

Proficiency with clinical trial management systems, start-up tracking tools, and standard business software systems. * Bachelor's degree in a scientific, health care, or related discipline, or ...

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All JobsClinical Trial Software JobsClinical Trial Software Jobs in Raleigh, NC

Clinical Trial Software information

See Raleigh, NC salary details

$11

$36

$66

How much do clinical trial software jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical trial software in Raleigh, NC is $36.62, according to ZipRecruiter salary data. Most workers in this role earn between $25.00 and $46.73 per hour, depending on experience, location, and employer.

What is clinical trial software?

Clinical trial software refers to specialized digital tools used to plan, manage, and monitor clinical trials in the medical and pharmaceutical fields. These platforms help streamline processes such as patient recruitment, data collection, regulatory compliance, and reporting. By automating many tasks, clinical trial software increases efficiency, reduces errors, and ensures adherence to industry standards and regulations. This technology is essential for organizations conducting clinical research, as it improves data accuracy and enhances collaboration among stakeholders.

How does a clinical trial software specialist typically collaborate with clinical research teams during a study?

A Clinical Trial Software Specialist works closely with clinical research coordinators, data managers, and principal investigators to ensure the software aligns with study protocols and regulatory requirements. They are responsible for configuring electronic data capture (EDC) systems, providing user training, troubleshooting technical issues, and ensuring data integrity throughout the trial. This collaborative environment requires strong communication skills and a proactive approach to problem-solving, as the specialist often acts as a liaison between technical and non-technical team members.

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

To thrive as a Clinical Trial Software Specialist, you need a solid understanding of clinical research processes, data management, and software development principles, often supported by a degree in life sciences, computer science, or a related field. Familiarity with electronic data capture (EDC) systems such as Medidata or Oracle Clinical, knowledge of regulatory compliance like GCP, and sometimes certifications like Certified Clinical Data Manager (CCDM) are typically required. Strong analytical thinking, problem-solving abilities, and effective communication set top performers apart in this role. These skills and qualities are crucial for ensuring accurate data collection, regulatory compliance, and smooth collaboration across clinical research teams.

What is the difference between Clinical Trial Software vs Clinical Research Coordinator?

AspectClinical Trial SoftwareClinical Research Coordinator
Primary RoleSoftware tools used to manage, track, and analyze clinical trial dataManages daily activities of clinical trials, including patient recruitment and data collection
Required SkillsTechnical knowledge of software systems, data management, and complianceClinical knowledge, organization, communication, and regulatory understanding
Work EnvironmentTechnology-focused, often in office or remote settingsHospital, clinic, or research facility
Industry UsageUsed by clinical trial teams, data managers, and IT professionalsEmployed directly by research institutions, hospitals, or pharmaceutical companies

While Clinical Trial Software involves the tools used to facilitate and manage clinical trials, Clinical Research Coordinators are the professionals who execute and oversee the trial processes. Both roles are essential in the clinical research industry but serve different functions—one focuses on software solutions, the other on trial management and coordination.

What cities near Raleigh, NC are hiring for Clinical Trial Software jobs?

Cities near Raleigh, NC with the most Clinical Trial Software job openings:

Clinical Trial Software jobs near you
Infographic showing various Clinical Trial Software job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $76,160 per year, or $36.6 per hour.

Senior Clinical Research Associate

410 ICR United States USA

Raleigh, NC • Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted yesterday

Job description

Senior CRA / CRA II - United States - Home Based

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 Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Willingness to travel as required (approximately 60%)
     

    #LI-LB1 #LI-REMOTE


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