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

Syneos Health

CTM - Future Roles (US)

Morrisville, NC · On-site

... and software to support the effective conduct of the clinical project data review and capture ... Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician ...

Syneoshealth

CTM - Future Roles (US)

Morrisville, NC · On-site

... and software to support the effective conduct of the clinical project data review and capture ... Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician ...

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

Clinical Trial Operations * Coordinate and manage complex clinical research studies, including drug ... software such as SAS, R, SPSS, NVivo, or Atlas.ti. Scientific Contribution * Participate in ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Clinical Trial Operations * Coordinate and manage complex clinical research studies, including drug ... software such as SAS, R, SPSS, NVivo, or Atlas.ti. Scientific Contribution * Participate in ...

Pluto Health

Clinical Project Manager

Durham, NC · On-site

$85K - $120K/yr

Collaborative across multiple groups * Healthcare and/or clinical trial experience: with ... Demonstrate proficiency in project management software and tools, including Microsoft Project or ...

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Showing results 21-40

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.

Clinical Research Assistant

Velocity Clinical Research, Inc.

Durham, NC • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago

Velocity Clinical Research rating

7.3

Company rating: 7.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

76th of 120 rated laboratories

Job description

Overview
Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.
As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.
Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.
Summary:
The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities.
Responsibilities
Duties/Responsibilities:
  • Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity's SOPs
  • Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations
  • With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations
  • Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
  • Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial
  • Enter source data into the sponsor's and/or vendor's data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator
  • Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team
  • Understand good documentation practices when collecting, transferring data to sponsor/CRO data capture systems and resolving queries under the direction of the Clinical Research Coordinator
  • Understand the informed consent process with emphasis on ensuring initial and ongoing consent of study subjects
  • Understand basic elements of regulatory documentation required to initiate, maintain and close a clinical research trial
  • Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person
  • Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
  • Ability to escalate potential patient safety issues such as adverse events, serious adverse events, and adverse events of special interest to the Clinical Research Team
  • Cleaning, organizing, and disinfecting the patient care, lab and lab equipment areas as needed
  • Prepare source document charts, copy and/or file medical records and study related documents as required.
  • Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls and updating patient tracking systems.
  • Other duties as assigned

Qualifications
Education/Experience:
  • High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry

Required Licenses/Certifications:
  • Phlebotomy if applicable and required by state law
  • Intramuscular dose administration and preparation if applicable and required by state law

Required Skills:
  • Demonstrated knowledge of medical terminology
  • Demonstrated ability to use the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
  • Understanding of verbal, written, and organizational skills
  • Demonstrated ability to work as a team player
  • Demonstrated ability to read, write, and speak English
  • Demonstrated ability to multi-task
  • Demonstrated ability to follow written guidelines
  • Demonstrated ability to be flexible/adapt as daily schedule may change rapidly

Required Physical Abilities:
  • Sit or stand for long periods of time
  • Communicate in person and by a telephone
  • Limited walking required
  • Limited to lifting up to 30 pounds

NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.

What Velocity Clinical Research employees say

Hours and flexibility

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