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Genetic Research Assistant Jobs in Colorado (NOW HIRING)

Research Assistant I

Aurora, CO · On-site

$19.30 - $22/hr

Research Operations * Endpoint and Specialty Services * Site Operations * Data Management * Quality ... genetic information, marital status, or any other status protected by applicable state or local law.

Research Assistant (part-time) 15-20 Hours per week to start then hours will ramp up Location ... genetic information, veteran status, marital status, or any other characteristic protected by ...

Research Assistant (part-time) 15-20 Hours per week to start then hours will ramp up Location ... genetic information, veteran status, marital status, or any other characteristic protected by ...

Research Assistant (part-time) 15-20 Hours per week to start then hours will ramp up Location ... genetic information, veteran status, marital status, or any other characteristic protected by ...

Research Assistant (part-time) 15-20 Hours per week to start then hours will ramp up Location ... genetic information, veteran status, marital status, or any other characteristic protected by ...

Research Assistant I

Aurora, CO · On-site

$19.50 - $27/hr

Research Operations * Endpoint and Specialty Services * Site Operations * Data Management * Quality ... genetic information, marital status, or any other status protected by applicable state or local law.

Research

Denver, CO · On-site

$19.29 - $55/hr

Research Assistant * Research Associate * Research Scientist These are non-benefited, part-time ... genetic information, military enlistment, or veteran status, and any other class of individuals ...

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Showing results 1-20

Genetic Research Assistant information

See Colorado salary details

$8

$23

$33

How much do genetic research assistant jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for genetic research assistant in Colorado is $23.04, according to ZipRecruiter salary data. Most workers in this role earn between $19.47 and $26.78 per hour, depending on experience, location, and employer.

What is a genetic research assistant?

A Genetic Research Assistant supports scientists in conducting genetic research by performing laboratory experiments, analyzing DNA samples, and maintaining lab equipment. They assist in data collection, sample preparation, and documentation to ensure accurate research outcomes. Responsibilities may include PCR, gel electrophoresis, sequencing, and other molecular biology techniques. This role is essential in advancing genetic studies, medical research, and biotechnological applications. Strong attention to detail and analytical skills are crucial for success in this position.

What are the typical daily responsibilities of a genetic research assistant?

As a Genetic Research Assistant, your typical day may involve preparing and conducting experiments, analyzing DNA or RNA samples, recording and interpreting data, and maintaining laboratory equipment. You may also be responsible for ordering supplies, managing sample inventories, and ensuring compliance with safety protocols. Collaboration with research scientists and team members is common, as you might assist in designing studies, troubleshooting procedures, or presenting findings. This role often involves both hands-on laboratory work and time spent managing and analyzing research data, offering a well-rounded experience in a dynamic lab setting.

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

To thrive as a Genetic Research Assistant, you need a strong background in biology or genetics, laboratory techniques, and data analysis, usually supported by a bachelor’s degree in a related field. Familiarity with laboratory information management systems (LIMS), PCR machines, DNA sequencing software, and possibly certifications in lab safety or molecular biology are important. Attention to detail, strong organizational skills, and the ability to communicate effectively within a research team are valuable soft skills for this position. These skills ensure accurate experimentation, reliable research results, and smooth collaboration in a fast-paced scientific environment.

How to get a job in genetic research?

To get a job as a genetic research assistant, candidates typically need a bachelor's degree in genetics, biology, or a related field, along with laboratory skills and familiarity with genetic analysis tools. Gaining experience through internships or research projects can improve prospects, and some positions may require knowledge of bioinformatics or molecular techniques. Certifications or advanced degrees can also enhance job opportunities in this field.

What qualifications do you need to be a genetic research assistant?

A genetic research assistant typically needs a bachelor's degree in genetics, biology, or a related field. Laboratory skills, familiarity with genetic analysis tools, and attention to detail are important, and some positions may require experience with specific techniques like PCR or DNA sequencing.

What are popular job titles related to Genetic Research Assistant jobs in Colorado?

For Genetic Research Assistant jobs in Colorado, the most frequently searched job titles are:

What cities in Colorado are hiring for Genetic Research Assistant jobs?

Cities in Colorado with the most Genetic Research Assistant job openings:

Infographic showing various Genetic Research Assistant job openings in Colorado as of August 2026, with employment types broken down into 69% Full Time, and 31% Part Time. Highlights an 100% In-person job distribution, with an average salary of $47,919 per year, or $23 per hour.

Research Assistant I

CPC Clinical Research

Aurora, CO • On-site

$19.30 - $22/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago


Job description

Responsibilities:
  • Serve as a floating resource to perform a variety of activities in support of the execution and management of projects and programs.
  • Based on business needs, may provide assistance to the following functional areas:
  • Research Operations
  • Endpoint and Specialty Services
  • Site Operations
  • Data Management
  • Quality Control
  • Trial Master File
  • Work closely with other team members to ensure timely completion of deliverables and resolution of issues.
  • Perform a variety of general administrative tasks such as filing, copying, and preparation of shipments for assigned projects.
  • Upload essential documents into eTMF system.
  • Perform quality control reviews of project-specific documentation and support submission of documents to the Trial Master File.
  • Assist in sending project supplies to study sites and tracking receipt of those supplies.
  • Assist in tracking receipt, entry, upload, reviews and feedback to investigational sites of endpoint testing.
  • Assist with query management.
  • Serve as a study coordinator for select projects as needed.
  • Assist with user access requests (including user reconciliation).
  • Perform general data review of study data in EDCs.
  • Additional activities as required.

Qualifications:
  • GED or HS Diploma required. Nursing or bachelor's degree preferred.
  • Minimum 1 year of professional experience (clinical research experience preferred). Higher degree may be considered in lieu of experience.
  • Proficiency in MS Office, particularly spreadsheet databases and word-processing.
  • Good communication and organizational skills.
  • Great attention to detail.
  • Ability to work with others in a manner that promotes group effort and achievement.
  • Ability to shift priorities quickly while ensuring accuracy and timely completion of tasks.
  • Ability to manage conflicts and resolve problems effectively.
  • Ability to follow direction to accomplish day-to-day tasks.
  • Ability to manage conflicts and resolve problems effectively.
  • Ability to follow direction to accomplish day-to-day tasks.

Posting deadline: This posting will remain open until filled. For best consideration, please apply by September 7, 2026.
Note: Viable applicants will be required to pass a background and education verification check.
About CPC:
CPC is an academic research organization that offers full service clinical trial design, oversight, and management with rapid access to Key Opinion Leaders in a variety of therapeutic areas. With over 30 years of experience, CPC has provided services to over 150 clinical trials in a variety of indications, with an emphasis on cardiovascular, wound healing, diabetes and more.
CPC has expertise in managing clinical trials from a variety of funding sources including Industry, NIH, and Investigator Initiated trials.
CPC Community Health focuses on innovative programs that reach into communities to help people find effective ways to become active, empowered and healthy. http://www.cpccommunityhealth.org/
CPC offers:
  • Comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)
  • Matching 401(k) plan (dollar for dollar up to 4% of your eligible compensation, fully vested immediately)
  • 11 paid holidays
  • 15 - 25 vacation days based on years of service
  • Paid sick time (2.67 hours accrued bi-weekly up to a maximum of 80 hours)
  • Monthly fun events (e.g. team building activities, games, charitable events, potlucks, picnics)
  • Flexible and remote work schedules

An Equal Opportunity Employer
CPC is dedicated to the principles of equal employment opportunity (EEO). CPC prohibits unlawful discrimination against applicants or employees on the basis of age 40 and over, race (including traits historically associated with race, such as hair texture and length, protective hairstyles), sex, sexual orientation, gender identity, gender expression, color, religion, creed, national origin, ancestry, disability, military status, genetic information, marital status, or any other status protected by applicable state or local law. It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors.
Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws. If you need assistance, please email our Human Resources team at careers@cpcmed.org.