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Weekend Clinical Research Jobs in Madison, MS (NOW HIRING)

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

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 ...

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 ...

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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Weekend Clinical Research information

See Madison, MS salary details

$39.9K

$87.3K

$153.8K

How much do weekend clinical research jobs pay per year?

As of Sep 2, 2026, the average yearly pay for weekend clinical research in Madison, MS is $87,329.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,900.00 and $99,700.00 per year, depending on experience, location, and employer.

What is a weekend clinical research?

A Weekend Clinical Research job involves conducting or supporting clinical trials on weekends, typically for medical or pharmaceutical research. Responsibilities may include patient recruitment, data collection, monitoring study protocols, and ensuring regulatory compliance. These roles are ideal for professionals looking for flexible work schedules while contributing to medical advancements. Weekend clinical research positions are often available at hospitals, research institutions, or pharmaceutical companies.

What are the key skills and qualifications needed to thrive in weekend clinical research?

To thrive in Weekend Clinical Research, you need a background in life sciences or healthcare, experience in clinical trial processes, and attention to detail. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and proficiency in using Microsoft Office Suite are often required. Strong organizational skills, effective communication, and the ability to work independently during off-hours are key soft skills. These capabilities are crucial to ensure accurate data collection, adherence to regulatory standards, and smooth collaboration with research teams outside standard work hours.

What does a typical weekend schedule look like for weekend clinical research?

Weekend Clinical Research roles often involve supporting ongoing clinical trials by assisting with patient visits, data entry, and documentation tasks that must be completed outside of regular business hours. You may work independently or as part of a small team, coordinating closely with principal investigators and other study staff to ensure continuity and compliance with study protocols. Flexibility and reliability are important, as your work ensures that weekend operations integrate seamlessly with weekday research activities. This role is ideal for candidates looking for part-time opportunities or those balancing other weekday commitments with their passion for clinical research.

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

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

What are popular job titles related to Weekend Clinical Research jobs in Madison, MS?

For Weekend Clinical Research jobs in Madison, MS, the most frequently searched job titles are:

What job categories do people searching Weekend Clinical Research jobs in Madison, MS look for?

The top searched job categories for Weekend Clinical Research jobs in Madison, MS are:

Weekend Clinical Research jobs near you
Infographic showing various Weekend Clinical Research job openings in Madison, MS as of August 2026, with employment types broken down into 85% Full Time, and 15% Part Time. Highlights an 100% In-person job distribution, with an average salary of $87,329 per year, or $42 per hour.

Clinical Research Coordinator

Amaris Consulting

Jackson, MS • On-site

$21.25 - $28/hr

Other

Posted 13 days ago

Job description

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 between investigators, sponsor, and site staff, ensuring the study is conducted in compliance with the protocol, Good Clinical Practice (GCP), regulatory requirements, and institutional policies.


Key Information:

  • Location: McComb, Mississippi, USA
  • Work Mode: hybrid
  • This is a part-time role requiring 2–3 days of work per week.
  • Length of contract: 4 months
  • Type of contract: C2C
  • Salary rate: 40-50 USD per hour


Key Tasks:

  • Coordinate patient enrollment activities
  • Collect, review, and maintain source documentation and study records
  • Enter study data into Electronic Data Capture (EDC) systems and resolve data queries
  • Maintain regulatory binders and essential study documentation
  • Prepare for and support sponsor monitoring visits, audits, and site inspections
  • Ensure participant safety, confidentiality, and protocol compliance throughout the study
  • Collaborate closely with investigators, radiology staff, and study teams to ensure protocol-required procedures are completed


Profile

Must-Haves:

  • Bachelor's degree in a related field
  • 5 years of Clinical Research Coordination experience
  • Experience conducting sponsored research studies
  • Strong understanding of ICH-GCP guidelines, FDA regulations, and IRB submissions
  • Experience with Electronic Data Capture (EDC) systems
  • Experience with Medidata Rave
  • Ability and willingness to travel on-site to support study activities
  • Strong organizational and communication skills
  • Experience in subject enrollment management, source documentation, data entry, adverse event reporting, site regulatory documentation, and query resolution

Nice-to-Haves:

  • Experience in an imaging environment (particularly CT) to support imaging-related study activities


Why choose us

  • An international community bringing together more than 110 different nationalities
  • An environment where trust is central: 70% of our leaders started their careers at the entry level
  • A strong training system with our internal Academy and more than 250 modules available
  • A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.)


Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

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