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Computer Science Research Assistant Jobs in Tyler, TX

micro1 AI

AI Training Specialist - Physics

Tyler, TX · On-site +1

$80 - $150/hr

... assistant professor, or senior research scientist. * Recent (last ~5 years) representative ... Reliable access to high-speed internet and a computer suitable for rigorous technical work.

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Computer Science Research Assistant information

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How much do computer science research assistant jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for computer science research assistant in Tyler, TX is $20.65, according to ZipRecruiter salary data. Most workers in this role earn between $17.45 and $23.99 per hour, depending on experience, location, and employer.

What is a computer science research assistant?

A Computer Science Research Assistant supports professors or researchers in conducting experiments, analyzing data, and developing software or algorithms. They may assist with literature reviews, coding, debugging, or testing to advance research projects. The role often involves working with programming languages, machine learning, cybersecurity, or other specialized topics. It provides valuable experience for students or professionals looking to deepen their knowledge in the field.

What are the typical duties and daily responsibilities of a computer science research assistant?

As a Computer Science Research Assistant, your daily responsibilities often include assisting with data collection and analysis, developing or testing software prototypes, conducting literature reviews, and helping prepare reports or presentations for research findings. You may also collaborate closely with faculty, graduate students, or industry partners, contributing to coding tasks, experimental setups, and troubleshooting technical issues as they arise. The role frequently involves both independent problem-solving and teamwork, providing a supportive environment to deepen technical skills and gain hands-on research experience. This position is an excellent opportunity to develop your research portfolio, learn advanced computing concepts, and prepare for potential graduate study or specialized tech careers.

What are the key skills and qualifications needed to thrive as a computer science research assistant?

To thrive as a Computer Science Research Assistant, you need strong analytical skills, proficiency in programming languages (such as Python, Java, or C++), and a solid understanding of algorithms and data structures, usually evidenced by coursework or a relevant degree. Familiarity with research tools, version control systems (like Git), and possibly certifications in data analysis or machine learning are advantageous. Excellent problem-solving abilities, attention to detail, and effective written and verbal communication help individuals excel when collaborating on research projects. These competencies enable you to support rigorous research, contribute to innovative solutions, and work efficiently as part of an academic or industry research team.

What are the most commonly searched types of Computer Science Research jobs in Tyler, TX?

The most popular types of Computer Science Research jobs in Tyler, TX are:

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For Computer Science Research Assistant jobs in Tyler, TX, the most frequently searched job titles are:

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What cities near Tyler, TX are hiring for Computer Science Research Assistant jobs?

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Computer Science Research Assistant jobs near you
Infographic showing various Computer Science Research Assistant job openings in Tyler, TX as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 76% Full Time, 19% Part Time, 2% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $42,943 per year, or $20.6 per hour.

Clinical Research Coordinator I - RN

Tyler, TX • On-site

Iterative Health
See more jobs at Iterative Healthexternal

$65K - $81K/yr

Full-time

Re-posted 7 days ago

Job description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
A Clinical Research Coordinator I - RN at Iterative Health is an essential member of the site research team, supporting, facilitating, and coordinating the daily execution of clinical trials across our network. This role is at the heart of every study - managing patient interactions, ensuring protocol compliance, maintaining data integrity, and keeping the operational machinery of clinical research running smoothly.
The ideal candidate brings clinical research experience, a patient-first mindset, strong attention to detail, and the ability to thrive in a fast-paced, protocol-driven environment. This role provides a strong foundation for success while offering a clear path for professional growth within Iterative Health's expanding site network.
Where You'll Drive Impact
  • Administratively and clinically manage industry-sponsored clinical trials, including problem-solving, communication, and protocol management.
  • Schedule all patient research visits and procedures in accordance with protocol requirements.
  • Ensure relevant study and subject-specific information is entered into the CTMS on a regular basis.
  • Complete and maintain study documentation including consent forms, source documentation, progress notes, case report forms, and investigational accountability forms.
  • Complete and maintain case report forms per FDA guidelines, reviewing them against patient medical records for completeness and accuracy.
  • Schedule and prepare for monitor visits.
  • Maintain inventory of study equipment and supplies onsite at all times.
  • Lead patient recruitment activities including chart reviews, protocol discussions with patients, and verification of informed consent documentation.
  • Conduct patient visits as outlined within each study protocol.
  • Act as the primary point of contact for study participants throughout the course of the study.
  • Dispense study medication, collect vital signs, and perform ECGs per protocol.
  • Perform blood draws; process and ship specimens per study protocol and IATA regulations.
  • As assigned: place IVs, administer IV medications and fluids, give intramuscular and subcutaneous injections, monitor patients during infusion, and discharge patients in accordance with protocol and site policies.
  • Adhere to Research SOPs, Good Clinical Practice (GCP) guidelines, and study protocols at all times.
  • Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocols.
  • Ensure all safety data is reviewed by the PI in a timely manner.
  • Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI; report instances of noncompliance to the appropriate compliance office.
  • Assist the study team in protecting the rights and welfare of all human research participants in accordance with federal regulations.
  • Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, and PI throughout the course of each study.
  • Actively participate in communication of status and results to management.
  • Perform job related duties as requested

What You Bring to the Team
  • Active Registered Nurse (RN) license required.
  • 1-2 years of clinical research experience strongly preferred .
  • Solid nursing background with a concentration in, or willingness to develop advanced knowledge of, GI specialty.
  • Ability to execute research tasks with guidance from experienced staff, PIs, and management.
  • Strong written and verbal communication skills.
  • Ability to read, interpret, and apply clinic policies and research protocols.
  • Proficiency in standard office software and CTMS platforms.
  • Highly organized with the ability to manage multiple priorities and meet deadlines.
  • Ability to work independently and collaboratively in a fast-paced environment.
Preferred Qualifications
  • Prior GI or hepatology clinical research experience.
  • Familiarity with GCP guidelines and FDA regulations governing clinical research.
  • Experience with CTMS, EDC, or eTMF platforms.
  • ACRP or SOCRA certification (CCRC or CCRP), or active pursuit of certification.

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.

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