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Weekend Research Assistant Jobs in Flowood, MS (NOW HIRING)

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 research team, working under the direction of the Principal Investigator and site management to support ...

Iterative Health

Research Assistant - Flowood, MS

Flowood, MS · On-site

$16.25 - $22.25/hr

We are seeking a full-time, on-site Research Assistant (RA). The RA is a specialized research professional working with and under the direction of the Clinical Principal Investigator (PI) and site ...

Iterative Health

Research Assistant - Flowood, MS

Flowood, MS · On-site

$16.25 - $22.25/hr

We are seeking a full-time, on-site Research Assistant (RA). The RA is a specialized research professional working with and under the direction of the Clinical Principal Investigator (PI) and site ...

Jackson State University

Research Associate

Jackson, MS · On-site

Support research and evaluation activities under the guidance of the Program Director. * Carry out additional project duties as assigned by the Program Director. * Collect data and manage databases ...

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 ...

New

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 ...

New

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All JobsResearch JobsWeekend Research Assistant JobsWeekend Research Assistant Jobs in Flowood, MS

Weekend Research Assistant information

What is a weekend research assistant?

A Weekend Research Assistant supports research projects by collecting, analyzing, and organizing data, typically working on weekends. Responsibilities may include conducting literature reviews, summarizing findings, assisting with experiments, or managing databases. This role is common in academic, scientific, and market research fields, offering flexible part-time work. Strong analytical skills, attention to detail, and research experience are often required.

What kind of responsibilities can I expect as a weekend research assistant?

As a Weekend Research Assistant, you may be responsible for tasks such as collecting and entering data, conducting literature reviews, maintaining lab equipment, and supporting ongoing experiments or studies. You'll often work independently, but regular communication with principal investigators, graduate students, or other research staff is common to ensure the integrity and progress of the research. This role often involves adhering to deadlines and managing multiple projects with precision, given the abbreviated weekend schedule. Gaining this experience can also provide valuable skills for future research or graduate-level positions.

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

To excel as a Weekend Research Assistant, you typically need strong analytical abilities, attention to detail, and a background in a relevant field such as science or social sciences, often backed by current enrollment in or completion of a degree program. Familiarity with research databases, data analysis software (such as SPSS or Excel), and good documentation practices are frequently required. Excellent time management, written communication, and independent problem-solving skills will help you stand out in this position. Mastery of these skills ensures efficient support for research projects, accurate data handling, and productive collaboration with research teams during limited weekend hours.

What job categories do people searching Weekend Research Assistant jobs in Flowood, MS look for?

The top searched job categories for Weekend Research Assistant jobs in Flowood, MS are:

What cities near Flowood, MS are hiring for Weekend Research Assistant jobs?

Cities near Flowood, MS with the most Weekend Research Assistant job openings:

Weekend Research Assistant jobs near you

Research Assistant - Wichita, KS

Flowood, MS

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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