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Research Associate Jobs in Canton, MS (NOW HIRING)

Research Assistant - Flowood, MS

Flowood, MS · On-site

$16.25 - $22.25/hr

The RA is a specialized research professional working with and under the direction of the Clinical Principal Investigator (PI) and site management. The primary responsibility of the RA is to assist ...

Clinical Research Coordinator

Jackson, MS · On-site

$21.25 - $28/hr

We are looking for an Clinical Research Coordinator to support the day-to-day management and execution of a clinical research study at an investigative site. You will serve as the primary liaison ...

Clinical Research Coordinator

Madison, MS · On-site

$19.75 - $26.25/hr

We are looking for an Clinical Research Coordinator to support the day-to-day management and execution of a clinical research study at an investigative site. You will serve as the primary liaison ...

Clinical Research Coordinator

Pearl, MS · On-site

$21 - $27.75/hr

We are looking for an Clinical Research Coordinator to support the day-to-day management and execution of a clinical research study at an investigative site. You will serve as the primary liaison ...

Clinical Research Coordinator 257479

Pearl, MS · On-site

$21 - $27.75/hr

Clinical Research Coordinators manage the daily operations of trials at the trial site. They work with patients, track data, and keep studies safe and legal. CRCs team up with doctors and cross ...

Clinical Research Coordinator 257479

Madison, MS · On-site

$19.75 - $26.25/hr

Clinical Research Coordinators manage the daily operations of trials at the trial site. They work with patients, track data, and keep studies safe and legal. CRCs team up with doctors and cross ...

Clinical Research Coordinator 257479

Jackson, MS · On-site

$21.25 - $28/hr

Clinical Research Coordinators manage the daily operations of trials at the trial site. They work with patients, track data, and keep studies safe and legal. CRCs team up with doctors and cross ...

Associate Attorney

Jackson, MS · On-site

$60K - $80K/yr

Our law firm has a full-time associate attorney position available now, and we're looking for the ... You'll also be responsible for performing legal research, drafting documents, and keeping client ...

Description Our law firm has a full-time associate attorney position available now, and we're ... You'll also be responsible for performing legal research, drafting documents, and keeping client ...

Associate Attorney

Jackson, MS · On-site

$120 - $180/hr

Superior research and writing skills. * Ability to multi-task. * Ability to analyze complex matters. Why Should You Apply? Our associates work closely with our senior lawyers and clients on ...

Showing results 21-40

Research Associate information

See Canton, MS salary details

$13

$27

$39

How much do research associate jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for research associate in Canton, MS is $27.67, according to ZipRecruiter salary data. Most workers in this role earn between $22.26 and $31.49 per hour, depending on experience, location, and employer.

What is a research associate?

Research Associates are professionals who support research projects in academic, scientific, or business settings. They assist with designing studies, collecting and analyzing data, and preparing reports or publications. Research Associates often work under the supervision of principal investigators or senior researchers, contributing their expertise to advance the goals of the project. Their responsibilities can vary depending on the field, but typically involve both administrative and hands-on research tasks.

What does a research associate do?

As a research associate, you conduct research and analysis as directed by a senior researcher or project manager. Researchers work in a number of fields, including medical science, the social sciences, natural sciences, finance, management, and academia. Your specific duties and responsibilities differ depending on the field in which you work, but some features of your work are similar across industries. You typically do primary and secondary source research, organize and process data, analyze said data, and report on your findings to lead researchers or clinicians.

What are the key skills and qualifications needed to thrive as a research associate, and why are they important?

To thrive as a Research Associate, you need a strong background in research methodology, data analysis, and subject-specific knowledge, typically supported by a relevant bachelor's or master's degree. Familiarity with statistical software (such as SPSS, R, or Python), laboratory equipment, and research databases is often essential. Attention to detail, critical thinking, and clear written and verbal communication skills set outstanding Research Associates apart. These skills ensure accurate data collection, effective collaboration, and the production of reliable, impactful research outcomes.

What are some typical challenges a research associate might face when managing multiple research projects simultaneously?

As a Research Associate, juggling multiple projects often requires strong organizational skills and the ability to prioritize tasks effectively. You might encounter challenges such as balancing deadlines, coordinating with various team members, and adapting to shifting project goals or data requirements. Effective communication and proactive time management are essential to ensure each project progresses smoothly and meets its milestones. Many teams use project management tools and regular check-ins to help mitigate these challenges and support collaboration.

What is the difference between Research Associate vs Research Scientist?

AspectResearch AssociateResearch Scientist
Required CredentialsBachelor's or Master's degree in relevant fieldMaster's or PhD in relevant field
Work EnvironmentLaboratories, research institutions, universitiesLaboratories, research institutions, industry settings
Employer & Industry UsageAcademic, government, non-profitAcademic, industry, biotech, pharma
Common Search & ComparisonYesYes

The main difference between a Research Associate and a Research Scientist lies in their educational requirements and level of experience. Research Associates typically hold a bachelor's or master's degree and assist in research projects, while Research Scientists usually have a PhD and lead research efforts. Both roles work in similar environments like labs and research institutions, but Research Scientists often have more independence and responsibility.

What qualifications do you need to be a research associate?

Research associates typically need a bachelor's degree in a relevant field such as science, engineering, or social sciences. Many positions prefer or require a master's degree or higher, along with strong analytical skills, proficiency with research tools, and experience in data collection and analysis.

What are the most commonly searched types of Research jobs in Canton, MS?

The most popular types of Research jobs in Canton, MS are:

What job categories do people searching Research Associate jobs in Canton, MS look for?

The top searched job categories for Research Associate jobs in Canton, MS are:

What cities near Canton, MS are hiring for Research Associate jobs?

Cities near Canton, MS with the most Research Associate job openings:

Infographic showing various Research Associate job openings in Canton, MS as of August 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $57,560 per year, or $27.7 per hour.

Research Assistant - Wichita, KS

Iterative Health

Flowood, MS

$16.25 - $22.25/hr

Full-time

Posted 14 days ago


Job description

The Research Assistant (RA) at Iterative Health is an essential on-site member of the clinical research team, working under the direction of the Principal Investigator and site management to support the day-to-day conduct of active clinical trials. 

This role assists Clinical Research Coordinators across every phase of study execution from participant screening and enrollment through documentation, data entry, and compliance. The ideal candidate is a detail-oriented, team-first professional with a healthcare background and a genuine interest in advancing clinical research. This role is a strong entry point into the clinical research field with real exposure to the full study lifecycle. 

Where You'll Drive Impact
  • Assist the Study Team with communicating study requirements to all individuals involved in the study.
  • Work with the Study Team to develop and implement recruitment strategies in accordance with site policies and IRB requirements.
  • Assist with screening subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility or exclusion.
  • Assist with registering participants in the Clinical Trial Management System (CTMS) to ensure proper billing of study procedures to the appropriate funding source.
  • Collect and report ongoing patient recruitment and enrollment progress and metrics to site management and the PI.
  • Assist the Study Team in completing study documentation and maintaining study files in accordance with sponsor requirements and site policies, including consent forms, source documentation, case report forms, and investigational material accountability forms.
  • Enter all patient visit data in eCRF and CTMS on a daily basis or as directed.
  • Arrange secure storage of study documents in accordance with GCP guidelines or the contracted length of time, whichever is longer.
  • Maintain inventory of study supplies; follow sponsor protocol and site policies on investigational drug/device accountability when applicable.
  • Process and ship specimens per study protocol and IATA regulations as directed.
  • Work with the Study Team to manage the day-to-day activities of the study, including problem-solving, communication, and protocol management.
  • Aid the Study Team in maintaining effective and ongoing communication with sponsors, research participants, site management, and the PI throughout the course of each study.
  • Assist the Study Team in protecting the rights and welfare of all human research participants in accordance with federal regulations.
  • Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI; report instances of noncompliance to the appropriate compliance office.
  • Perform job related duties as requested 

What You Bring to the Team

  • High school diploma or equivalent required; some college coursework preferred.
  • Minimum 2 years of experience in a healthcare setting.
  • Strong written and verbal communication skills.
  • Ability to read, interpret, and apply clinic policies and research protocols.
  • Proficiency in standard office software; familiarity with CTMS or eCRF platforms a plus.
  • Highly organized with the ability to manage multiple tasks and meet deadlines.
  • Ability to work both independently and collaboratively as part of a research team.
  • Professional, detail-oriented, and committed to maintaining confidentiality and data integrity.
Preferred Qualifications
  • Prior clinical research experience or exposure to clinical trial operations.
  • Familiarity with GCP guidelines and human subject research regulations.
  • Experience with specimen processing and shipping per IATA regulations.
  • Interest in pursuing a career path in clinical research coordination or research operations.
Physical Requirements
  • Ability to sit, stand, and move throughout clinical and office environments for extended periods of time
  • Ability to lift and move up to 25 pounds as needed