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Clinical Research Assistant Jobs in Ridgeland, MS

Iterative Health

Research Assistant - Wichita, KS

Flowood, MS · On-site

$16.25 - $22.25/hr

The Research Assistant (RA) at Iterative Health is an essential on-site member of the clinical ... This role assists Clinical Research Coordinators across every phase of study execution from ...

Iterative Health

Research Assistant - Wichita, KS

Flowood, MS · On-site

$16.25 - $22.25/hr

By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ... The Research Assistant (RA) at Iterative Health is an essential on-site member of the clinical ...

Iterative Health

Research Assistant - Flowood, MS

Flowood, MS · On-site

$16.25 - $22.25/hr

By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ... We are seeking a full-time, on-site Research Assistant (RA). The RA is a specialized research ...

Iterative Health

Research Assistant - Flowood, MS

Flowood, MS · On-site

$16.25 - $22.25/hr

The primary responsibility of the RA is to assist the Clinical Research Coordinators with conduct of research studies. The RA supports and facilitates the daily clinical trial activities and plays a ...

Amaris Consulting

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 ...

Amaris Consulting

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 ...

Amaris Consulting

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 ...

Medix™

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 ...

Medix™

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 ...

Medix™

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 ...

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Clinical Research Assistant information

See Ridgeland, MS salary details

$6

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How much do clinical research assistant jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for clinical research assistant in Ridgeland, MS is $18.92, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $21.63 per hour, depending on experience, location, and employer.

What is a clinical research assistant?

Clinical Research Assistants are professionals who support clinical research studies by performing a range of administrative and research-related tasks. They help collect and manage data, assist with patient recruitment, prepare study materials, and ensure compliance with research protocols and regulations. Their work is crucial in advancing medical knowledge and ensuring that clinical trials run smoothly and ethically. Clinical Research Assistants often work under the supervision of principal investigators or clinical research coordinators in hospitals, universities, or pharmaceutical companies.

What does a clinical research assistant do?

A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.

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

To thrive as a Clinical Research Assistant, you need a bachelor’s degree in a life science or health-related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) certification are typically required. Excellent communication, teamwork, and problem-solving abilities help you excel in coordinating with research teams and participants. These skills ensure accurate data collection, regulatory compliance, and the smooth execution of clinical studies.

What are some common challenges clinical research assistants face when coordinating multiple studies simultaneously?

Clinical Research Assistants often manage several studies at once, which can lead to challenges in balancing competing deadlines, maintaining accurate documentation, and ensuring compliance with complex protocols. Effective time management and organizational skills are crucial to handle overlapping tasks such as scheduling patient visits, collecting data, and preparing regulatory submissions. Collaborating closely with principal investigators, coordinators, and other team members helps distribute the workload and maintain research quality. Developing strong communication habits and utilizing digital tracking tools can further streamline workflow and reduce errors.

What is the difference between Clinical Research Assistant vs Clinical Research Coordinator?

AspectClinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentAssists in data collection, patient scheduling, and administrative tasks in clinical trial settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trial sites
Employer & IndustryHospitals, research institutions, pharmaceutical companiesHospitals, research centers, pharmaceutical companies

Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

Can you be a clinical research assistant with no experience?

Clinical research assistant positions often require some knowledge of medical terminology and data management, but many entry-level roles are available for candidates without prior experience. Employers may provide on-the-job training and look for strong organizational skills, attention to detail, and the ability to follow protocols. Certifications such as Good Clinical Practice (GCP) can enhance prospects for those new to the field.
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The top searched job categories for Clinical Research Assistant jobs in Ridgeland, MS are:

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Clinical Research Assistant jobs near you
Infographic showing various Clinical Research Assistant job openings in Ridgeland, MS as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 20% Part Time, and 6% Contract. Highlights an 83% Physical, 1% Hybrid, and 16% Remote job distribution, with an average salary of $39,360 per year, or $18.9 per hour.

Research Assistant - Wichita, KS

Flowood, MS • On-site

Iterative Health
See more jobs at Iterative Healthexternal

$16.25 - $22.25/hr

Full-time

Posted 10 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

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