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Cra Computer Science Jobs (NOW HIRING)

IQVIA

Clinical Research Associate

Overland Park, KS · On-site

$71K - $189K/yr

Qualifications Bachelor's Degree Degree in scientific discipline or health care preferred ... Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a ...

IQVIA

Clinical Research Associate, Full Service

Durham, NC · On-site

$47K - $169K/yr

Qualifications Bachelor's Degree Degree in scientific discipline or health care preferred. Req ... Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a ...

Emerson

DevOps Engineer- Azure/Programming

Shakopee, MN · On-site

$108K - $120K/yr

Bachelor's degree in Engineering, Computer Science, or a related field * Minimum five (5) years of ... CRA, IEC 62443) Our Culture & Commitment to You: At Emerson, we prioritize a workplace where every ...

IQVIA

Clinical Research Associate

Carlsbad, CA · On-site

$71K - $189K/yr

Qualifications Bachelor's Degree Degree in scientific discipline or health care preferred ... Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a ...

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All JobsCra Computer Science Jobs

CRA Computer Science information

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$11K

$79.4K

$137.5K

How much do cra computer science jobs pay per year?

As of Aug 5, 2026, the average yearly pay for cra computer science in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a CRA Computer Science?

To thrive as a CRA in Computer Science, you generally need a strong background in computer science or related fields, with expertise in data analysis, clinical trial protocols, and regulatory compliance. Familiarity with electronic data capture (EDC) systems, clinical trial management software, and GCP (Good Clinical Practice) certification are typically required. Exceptional attention to detail, strong organizational skills, and effective communication are crucial soft skills for this role. These competencies ensure accurate data management, regulatory adherence, and successful collaboration across research teams and stakeholders.

What is the difference between Cra Computer Science vs Software Developer?

CriteriaCra Computer ScienceSoftware Developer
Required CredentialsBachelor's in Computer Science or related field; certifications like CompTIA, CiscoBachelor's in Computer Science or related field; certifications like Microsoft, AWS
Work EnvironmentGovernment agencies, research labs, educational institutionsPrivate companies, tech startups, software firms
Employer & Industry UsagePrimarily in government and academiaPrimarily in tech industry and private sector
Common Search & ComparisonYesYes

Cra Computer Science and Software Developer roles share similar educational backgrounds and certifications. However, Cra Computer Science often focuses on research, government projects, and academia, while Software Developers typically work in private sector tech companies creating applications and software solutions. Both roles require strong programming skills but differ in work environment and industry focus.

What is a CRA Computer Science?

CRA Computer Science professionals are individuals who work in the field of computer science, often associated with the Computing Research Association (CRA). They may be researchers, faculty, or students engaged in advancing computer science through research, education, and advocacy. The CRA is a key organization that supports the computing research community by organizing conferences, providing resources, and fostering collaboration among academic, government, and industry professionals. CRA Computer Science professionals are dedicated to pushing the boundaries of technology and innovation.

Is a CRA computer science career in demand?

A CRA computer science career is in high demand due to the growing need for technology professionals across industries. Skills in programming, data analysis, and cybersecurity increase employability, and many roles offer competitive salaries and opportunities for advancement.

What are common challenges faced by CRAs with a computer science background when transitioning into clinical research roles?

CRAs with a computer science background may initially face challenges in adapting to the highly regulated environment of clinical research, including understanding protocols, compliance requirements, and ethical considerations. While their technical skills are valuable for data management and electronic systems, they may need to quickly learn clinical terminology and regulatory guidelines. Collaborating with clinical teams and effectively communicating complex technical concepts to non-technical colleagues are also common hurdles. With proper onboarding and ongoing training, CRAs can leverage their computer science expertise to streamline data processes and contribute significantly to study success.
More about CRA Computer Science jobs
What cities are hiring for Cra Computer Science jobs? Cities with the most Cra Computer Science job openings:
What job categories do people searching Cra Computer Science jobs look for? The top searched job categories for Cra Computer Science jobs are:
CRA Computer Science jobs near you
Infographic showing various Cra Computer Science job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

In-House CRA / Clinical Trial Associate

REGENXBIO

Rockville, MD • On-site

$34.25 - $46.75/hr

Full-time

Retirement

Re-posted 15 days ago

Job description

The opportunity:
As the In-house CRA you will support and coordinate the logistical aspects of clinical trial management, site management, data review and cleaning according to FDA regulations, Good Clinical Practice (GCP) and relevant SOPs and acts as a pivotal point of contact for the clinical trial team. Under general supervision, you will assist with the coordination of activities associated with the start-up, conduct, and close-out of clinical trials and other duties as assigned. Although prior CRA experience is not essential, a working knowledge of the clinical trial process and associated regulations, responsibilities, and roles are required.
What you'll be doing:
  • Assists in the development and editing of study-related materials (e.g. consent forms, study binders, site study aids)
  • Assists with preparation of training workshops, Investigator/Advisory Board meeting materials
  • Assists with all phases of clinical trial activities (e.g. start-up, conduct, and close-out)
  • Develops study tracking tools (e.g. site lists, enrollment tracking, vendor spreadsheets)
  • Maintains tracking spreadsheets/databases and provides routine reports/dashboards to study team members
  • Requests PO independently, may review invoices with oversight from Clinical Project Manager (CPM)
  • Tracks essential documents and maintains/reviews the eTMF under the guidance of CPM.
  • Assists with management of investigational product and study supplies by ensuring the accuracy of shipments of study-related materials and collection of regulatory documents required for IP release
  • May attend co-monitoring visits or other site visits based on experience and training provided by and under guidance of CPM or designee
  • Assists the CPM with the review of clinical database and management of flow of data, including but not limited to facilitating resolution of queries
  • Assists with collection, review and filing of regulatory and other essential documents from clinical personnel (e.g. site trip reports) and sites (e.g. FDA 1572 reports)
  • Assists with filing and management of the Electronic Trial Master File (eTMF)
  • Distributes meeting's agenda, prepare and distributes final meeting minutes including documentation of action items
  • May assume a specialized administrative role (e.g. SOP Administrator)
  • Travel up to 5% of the time is required
  • It is imperative that REGENXBIO employees embody our core values by working collaboratively, building strong relationships and using clear communication to meet shared objectives.

What we're looking for:
We set our employees up for success. To be successful in this role and help us achieve our goals, we are looking for someone with the following skills and qualifications:
  • A Bachelor's degree (BA or BS) with an emphasis on scientific discipline or related healthcare field preferred, however, the combination of experience working in clinical research field and training will be taken under consideration.
  • 1-2 years applicable experience in a pharmaceutical, biotechnology, CRO and /or healthcare setting required
  • Knowledgeable of clinical research operations, including interpretation and implementation of FDA regulations, GCP/ICH R2
  • Demonstrate core understanding of medical terminology or clinical trial activities
  • Must have working knowledge and understanding of clinical protocols, and all other associated study related documents
  • Advanced knowledge of Word, Excel and Power Point and Outlook
  • Knowledge of the principles and practices of computer applications in database management
  • Must have a high degree of customer focus toward internal and external stakeholders
  • Must display strong analytical and problem-solving skills
  • Strong interpersonal and relationship management with the cross-functional team and external vendors skills
  • Clear and concise verbal and written communication skills
  • Attention to detail and organizational skills required
  • Ability to establish priorities, excellent sense of urgency to manage multiple tasks and deadlines

Why should you apply?
By joining REGENXBIO, you will have the opportunity to be a part of a growing company, with an incredible team, who is passionate about developing novel AAV gene therapies for patients in need.
We offer a comprehensive and competitive benefit & compensation package which includes market-competitive salaries, an annual bonus program, education assistance, retirement plan with employer match, stock options at all levels, summer hours and more!
In addition, professional development is important to us. By joining our team, you'll have the opportunity to be exposed to challenging projects and have access to development resources to help you grow personally and professionally.
Qualifications
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Education
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Preferred
Bachelor of Science (B.S.) or better.
Skills & Requirements Qualifications

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