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Clinical Trial Software Jobs (NOW HIRING)

Clinical Ink

Validation Analyst

Ensure the correct functioning of clinical trial software with focus on patient safety and integrity of clinical study data by: * Ensuring requirements are clear, testable, and consistent with the ...

Suvoda

Senior Software Developer

Conshohocken, PA · On-site

$53.75 - $70.75/hr

Suvoda is a global clinical trial technology company shaping digital experiences that enable ... As a Software Developer on Suvoda's Product team, you'll design and build clinical trial software ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Knowledge of project management tools and practices and proficiency in using normal office software:

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Knowledge of project management tools and practices and proficiency in using normal office software:

Kailera Therapeutics, Inc.

Clinical Trial Manager

Waltham, MA · On-site

$127K - $155K/yr

  • Medical

  • Life

  • Retirement

The Clinical Trial Manager will provide project support to team members by leading and/or ... Advanced proficiency in Microsoft Office and Microsoft Project or other Project Management software

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Senior Clinical Research Associate

Wilmington, 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 ...

Actalent

Clinical Trial Specialist

Newark, NJ

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Use clinical trial management systems and software such as Excel and Word to develop and maintain study tools, documentation templates, and tracking systems. * Collaborate with the Research Nurse ...

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Senior Clinical Research Associate

New York, NY

$110K - $138K/yr

  • 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

Senior Clinical Research Associate

Rochester, NY · On-site

$110K - $138K/yr

  • 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

Hickory, 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

Wilmington, 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 Clinical Research Associate

Downers Grove, IL · 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 ...

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All JobsClinical Trial Software Jobs

Clinical Trial Software information

See salary details

$11

$37

$68

How much do clinical trial software jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical trial software in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

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 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.

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 are hiring for Clinical Trial Software jobs?

Cities with the most Clinical Trial Software job openings:

What states have the most Clinical Trial Software jobs?

States with the most job openings for Clinical Trial Software jobs include:

Clinical Trial Software jobs near you
Infographic showing various Clinical Trial Software job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Validation Analyst

Clinical Ink

Remote

Full-time

Re-posted 10 days ago

Job description

Company Information
Clinical Ink is the global life science company that brings data, technology, and patient science together to unlock clinical discovery. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancement, drive the industry standard for data precision and usher in a new generation of clinical trials. With offices in the United States and Denmark, Clinical Ink is rewriting the clinical development experience.
Job Description
Clinical Ink is seeking a Validation Analyst to join our Project Quality team based remotely across the United States! This individual will contribute to developing and overseeing the execution of test scripts for clinical trial software. The Validation Analyst's responsibilities include:
  • Develop and oversee the execution of testing scripts
  • Ensure the correct functioning of clinical trial software with focus on patient safety and integrity of clinical study data by:
    • Ensuring requirements are clear, testable, and consistent with the clinical trial
      protocol
    • Proofreading requirements for spelling and congruency with clinical trial protocol
    • Scripting and/or conducting protocol/project specific testing to ensure fulfillment of study design, build, and implementation requirements
    • Documenting testing in accordance with applicable process and procedures
    • Executing qualification testing on section build requirements
    • Executing qualification testing on form design requirements
    • Documenting defects and tracking to resolution
    • Verifying approved study-specific configuration settings
  • As required, assist with the execution of platform testing
  • Provide cross-functional support to Data Quality, as needed, including:
    • Verify and validate data reports and exports
    • Verify data clarifications
  • Perform other related duties as assigned
Qualifications
  • Associates degree or relevant experience
  • Strong written/verbal communication skills; ability to communicate with personnel at various levels
  • Exceptional computer skills; proficiency with Microsoft Word, Excel, etc.
  • Detail-oriented and analytical reasoning skills
  • Sense of ownership and proactive approach to work
  • Effective prioritization, time management, and organizational skills

Additional Information
Clinical ink is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status.
www.clinicalink.com ​

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