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Cra Computer Science Jobs (NOW HIRING)

Alira Health

$85K - $125K/yr

... scientific, and other meetings as required. * Assists in CRA new hire training and onboarding ... Good computer skills, with ability to use clinical trial management systems, clinical trial ...

Emmes

Clinical Research Associate II

Rockville, MD · On-site +1

The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable ... Excellent computer and organizational skills. * High level of attention to detail required.

Novotech

Clinical Research Associate

$70K - $110K/yr

The CRA is the primary contact between the Investigational Sites, Novotech, and Sponsor. Key ... Qualifications Graduate in a clinical or life sciences-related field. Relevant experience ...

Thermo Fisher Scientific

Assistant CRA

Cornelius, NC · Hybrid

Education and Experience Requirements: • Bachelor's degree in a life science discipline or ... • Proficient computer skills with good knowledge of MS Office ability to learn and use ...

Qualcomm

Senior Security System Test Engineer

San Diego, CA · On-site

$121K - $166K/yr

... Act (CRA). • Works across multiple disciplines from system architects, hardware designers ... Computer Science or related degree field. • Bachelor's Degree (or foreign academic equivalent) in ...

AstraZeneca

Clinical Research Associate

Wilmington, DE · On-site

Bachelor's degree, preferably in Life Science discipline * 1.5+ years of CRA experience in ... Ability to understand the impact of technology on projects and to use and develop computer skills ...

AstraZeneca

Clinical Research Associate

Wilmington, DE · On-site

Bachelor's degree, preferably in Life Science discipline * 1.5+ years of CRA experience in ... Ability to understand the impact of technology on projects and to use and develop computer skills ...

AstraZeneca

Clinical Research Associate

Wilmington, DE · On-site

Bachelor's degree, preferably in Life Science discipline * 1.5+ years of CRA experience in ... Ability to understand the impact of technology on projects and to use and develop computer skills ...

AstraZeneca

Clinical Research Associate

Wilmington, DE · On-site

Bachelor's degree, preferably in Life Science discipline * 1.5+ years of CRA experience in ... Ability to understand the impact of technology on projects and to use and develop computer skills ...

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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 Jul 15, 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 (Clinical Research Associate) in Computer Science, and why are they important?

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.

Is a CRA career in demand?

A CRA (Clinical Research Associate) career is in demand due to the growth of clinical trials and the pharmaceutical industry. CRAs are essential for monitoring clinical studies, and demand is expected to increase with advancements in medical research and regulatory requirements. Strong knowledge of Good Clinical Practice (GCP) and relevant certifications can enhance job prospects.

What are CRA Computer Science professionals?

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.

What jobs can I get after being a CRA?

A Clinical Research Associate (CRA) can transition into roles such as Clinical Project Manager, Clinical Data Manager, Regulatory Affairs Specialist, or Quality Assurance Auditor. These positions often require knowledge of clinical trial processes, regulatory guidelines, and data management tools, and may involve certifications like CCRP or RAC.

What are some common challenges faced by Clinical Research Associates (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.

What is the CRA in CS?

In computer science, CRA typically refers to a Certified Research Associate or a similar role involving research and development. It often requires strong programming skills, knowledge of algorithms, and familiarity with research methodologies or specific tools depending on the organization. The term can vary based on context, so it's important to clarify the specific role or organization.

Is it hard to get a CRA job?

A CRA (Clinical Research Associate) job can be competitive, requiring relevant education, such as a degree in life sciences or related fields, and experience with clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like CCRP can improve chances, but the hiring process often involves multiple interviews and assessments of technical knowledge.
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, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 82% Physical, 1% Hybrid, and 17% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.
Clinical Research Associate

Clinical Research Associate

Alira Health

On-site, Remote

$85K - $125K/yr

Full-time

Posted 2 days ago

Job description

🔗Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you.
Join our global team dedicated to innovation and initiative, where physical walls and different time zones don't limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.
Job Description Summary
The CRA is an important member of the Alira Health Clinical team. The CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality. The CRA works closely with Lead CRAs, Sr CRAs, in-house CRAs, Associate Director of Clinical Monitoring and Project Managers to ensure protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues.
Job Description
KEY RESPONSABILITIES
  • Provides guidance, oversight, and feedback to the CRA team to ensure adherence to project scope, SOPs, timelines, and budget requirements.
  • Reviews monitoring visit reports, conducts co-monitoring and evaluation visits as needed.
  • Ensures appropriate and timely investigator site visits.
  • Coordinates with appropriate cross-functional departments to facilitate negotiation/issue resolution for clinical trial monitoring related issues.
  • Assists in development of study-specific Monitoring Plans and training presentations as required.
  • Assists in set up/collection of site specific ethics documents and site contract negotiation as required.
  • Provides monthly billing information to finance team as required.
  • For monitoring stand-alone projects, manages study budget and acts as referent for the sponsor.
  • Performs qualification, initiation, interim, and close-out visits both remotely and onsite, ensuring proper documentation of monitoring visits.
  • Prepares consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status.
  • Ensures integrity of CRF data through meticulous and thorough source document review and verification.
  • Performs quality control and verification of documents collected at sites for eTMF/TMF.
  • Conducts investigational product accountability.
  • Reviews site regulatory binder for required documents.
  • Maintains regular contact with study sites to ensure protocol/GCP compliance, assesses patient accrual rates, and responds to sponsor requests.
  • Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company/Sponsor SOPs.
  • Participates in internal, client/sponsor, scientific, and other meetings as required.
  • Facilitates adverse event reporting and ensures the reconciliation of SAE reports with source documentation and CRFs.
  • Works closely with in-house CRAs/CTC and data management to resolve queries on discrepant data.
  • Proactively identifies site issues and develops problem-solving strategies for sites.
  • Conducts audit preparation at study sites as needed.
  • Works with other CRAs to maintain consistency and promote a collaborative team atmosphere.
  • Participates in internal, client/sponsor, scientific, and other meetings as required.
  • Assists in CRA new hire training and onboarding.
  • Performs CRA mentoring.
  • Collaborates with development and maintenance of Clinical Trial Management System (CTMS).
  • Manages and resolves conflicting priorities to deliver on commitments.
  • Performs additional duties as assigned.

Compensation: $85,000 - 125,000 commensurate with experience
DESIRED QUALIFICATION & EXPERIENCE
  • EU: Graduation in a scientific health field
  • EU (Italy): Certified Monitor in compliance with Italian CRO decree dated 15Nov2011
  • Ability to establish and maintain positive relationships with Sponsor, Site and Project Team members
  • Ability to autonomously manage monitoring activities

TECHNICAL COMPETENCES & SOFT SKILLS
  • Quality focused; Proven ability to be careful, thorough, and detail-oriented
  • Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment
  • Able to manage priorities, organize time and solve problems
  • Strong analytical, negotiation, meeting management, cross-functional team, and leadership skills
  • Ability to travel
  • Ability to manage stress
  • Professional, trustworthy and disciplined
  • Ability to problem-solve unstructured or ambiguous challenges
  • Strong command of Local language, both written and verbal, in the country where monitoring activities are performed
  • Excellent communication and interpersonal skills with customer service orientation
  • Good computer skills, with ability to use clinical trial management systems, clinical trial databases and electronic data capture
  • Self-starter who thrives in a collaborative, yet less structured team environment
  • Knowledge of clinical research, ICH GCP and local regulations
  • Knowledge of Regulatory and Ethical requirements
  • EU: Adequate English

Languages
English
Education
Bachelor of Science (BS): Biology, Bachelor of Science (BS): Life Sciences
Contract Type
Regular
Salary Range
The final offer will be determined within the applicable location-specific range and will depend on the candidate's confirmed work location, relevant experience, skills, qualifications, internal equity, and role scope.

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