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Computer Science Research Assistant Jobs in Worcester, MA

We are seeking a Research Associate II to support analytical development activities within a ... Troubleshoot routine technical issues and assist with method optimization activities Data Analysis ...

Research Technician

Chepachet, RI

$20.25 - $28/hr

... scientific research capability and engineering expertise are solely dedicated to property risk ... and computer literacy. Must be able to commute to the FM Research Campus in West Glocester, RI.

... scientific research capability and engineering expertise are solely dedicated to property risk ... and computer literacy. Must be able to commute to the FM Research Campus in West Glocester, RI.

Research Technician

RI · On-site

$26.71/hr

... scientific research capability and engineering expertise are solely dedicated to property risk ... and computer literacy. Must be able to commute to the FM Research Campus in West Glocester, RI.

Research Technician

Chepachet, RI

$20.25 - $28/hr

... scientific research capability and engineering expertise are solely dedicated to property risk ... and computer literacy. Must be able to commute to the FM Research Campus in West Glocester, RI.

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Computer Science Research Assistant information

See Worcester, MA salary details

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

As of Jun 10, 2026, the average hourly pay for computer science research assistant in Worcester, MA is $21.86, according to ZipRecruiter salary data. Most workers in this role earn between $18.46 and $25.43 per hour, depending on experience, location, and employer.

What is a Computer Science Research Assistant job?

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 key skills and qualifications needed to thrive in the Computer Science Research Assistant position, and why are they important?

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 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 popular job titles related to Computer Science Research Assistant jobs in Worcester, MA? For Computer Science Research Assistant jobs in Worcester, MA, the most frequently searched job titles are:
What job categories do people searching Computer Science Research Assistant jobs in Worcester, MA look for? The top searched job categories for Computer Science Research Assistant jobs in Worcester, MA are:
What cities near Worcester, MA are hiring for Computer Science Research Assistant jobs? Cities near Worcester, MA with the most Computer Science Research Assistant job openings:
Infographic showing various Computer Science Research Assistant job openings in Worcester, MA as of June 2026, with employment types broken down into 1% As Needed, 72% Full Time, 23% Part Time, and 4% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $45,472 per year, or $21.9 per hour.
Scientific Coordinator - Bioanalytical Chemistry

Scientific Coordinator - Bioanalytical Chemistry

Charles River Laboratories, Inc.

Shrewsbury, MA • On-site

$29/hr

Other

Medical, Retirement, PTO

Posted 6 days ago


Charles River Laboratories rating

8.2

Company rating: 8.2 out of 10

Based on 90 frontline employees who took The Breakroom Quiz

26th of 71 rated pharmaceutical


Job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.

Job Overview

Provide protocol and direct support to Research Scientist and Sponsors with all aspects of data management. Assist with management of QA audit and assure necessary corrections and follow-up take place.

Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Interact regularly with Research Scientists and Sponsors: respond to sponsor-requests for information.

Assure a full understanding of assigned projects and results, including objectives, timelines and reporting requirements.

For clinical studies:

Maintain master inventory list.

 Document and communicate discrepancies to Sponsor and resolve as appropriate.

 Work with Sponsors, Data Managers and Research Scientist to coordinate data transfer agreements.

Create data transfer files and provide to Sponsor and Data Managers. Reconcile discrepancies as needed.

Tabulate study data and generate report tables.

Extract information from study data to generate results and conclusions in conjunction with the Research Scientist.

Under direction of the Research Scientist, receive, review and QC reports and make recommended corrections as appropriate.

Assemble data package and ensure data is GLP compliant prior to QA submission.

Assist with QA audits and assure necessary corrections and follow-up take place.

Support in documentation of deviations and help in drafting new SOPs. Assist in the maintenance and communication of departmental systems and SOPs.

Perform all other related duties as assigned.

The pay range for this position is $29.00/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

QUALIFICATIONS:

Education: Bachelor's degree (B.A./B.S.) or equivalent in science or related discipline.

Experience: 2-4 years related experience in a laboratory or scientific research

environment. This position requires analytical thinking skills and a good understanding

of scientific processes.

An equivalent combination of education and experience may be accepted as a

satisfactory substitute for the specific education and experience listed above.

Certification/Licensure: None.

Other: Knowledge of Good Laboratory Practice (GLP) regulations. Familiar with scientific

protocols and reports and all components required for completeness. Computer skills

including MS Office software and database management. Strong organizational skills and

attention to detail.

Education
Four-year degree required
Physical Requirements

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market.  Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.


About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We're committed to providing benefits that elevate your quality of life.  Based on your position these may include:  bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.


What Charles River Laboratories employees say

Pay

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About Charles River

Sourced by ZipRecruiter

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947