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Weekend Clinical Research Jobs in Kansas (NOW HIRING)

Tekton Research Inc

Clinical Research Coordinator

Wichita, KS · On-site

$21.50 - $28.75/hr

Clinical Research Coordinator (CRC) About Tekton Research: Tekton Research is a growth-oriented clinical research organization committed to conducting high-quality clinical trials that advance ...

Grene Vision Group

Clinical Research Coordinator

Wichita, KS · On-site

$21.75 - $28.75/hr

Clinical Research Coordinator DEPARTMENT: Clinical Research LOCATION: Wichita, KS PERKS * Full Benefits Package - Medical, Vision, Dental and Life Insurance * 401k + Employer Matching * Paid Time Off ...

Grene Vision Group

Clinical Research Coordinator

Wichita, KS

$21.75 - $28.75/hr

Clinical Research Coordinator DEPARTMENT: Clinical Research LOCATION: Wichita, KS PERKS * Full Benefits Package - Medical, Vision, Dental and Life Insurance * 401k + Employer Matching * Paid Time Off ...

Medix

Clinical Research Nurse

Overland Park, KS · On-site

$38 - $42/hr

Job Summary Our client is seeking a Clinical Research Nurse to join their diverse team. The primary role includes overseeing critical phase 1/2 clinical trials, ranging from standard medical to ...

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Weekend Clinical Research information

See Kansas salary details

$43.7K

$95.7K

$168.6K

How much do weekend clinical research jobs pay per year?

As of Aug 7, 2026, the average yearly pay for weekend clinical research in Kansas is $95,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,200.00 and $109,300.00 per year, depending on experience, location, and employer.

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 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 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 Kansas? The most popular types of Clinical Research jobs in Kansas are:
What are popular job titles related to Weekend Clinical Research jobs in Kansas? For Weekend Clinical Research jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Weekend Clinical Research jobs in Kansas look for? The top searched job categories for Weekend Clinical Research jobs in Kansas are:
What cities in Kansas are hiring for Weekend Clinical Research jobs? Cities in Kansas with the most Weekend Clinical Research job openings:
Weekend Clinical Research jobs near you
Infographic showing various Weekend Clinical Research job openings in Kansas as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $95,728 per year, or $46 per hour.

Clinical Research Coordinator

Tekton Research Inc

Wichita, KS • On-site

$21.50 - $28.75/hr

Full-time

Posted 7 days ago

Job description

Clinical Research Coordinator (CRC)

About Tekton Research:

Tekton Research is a growth-oriented clinical research organization committed to conducting high-quality clinical trials that advance medical knowledge and improve patient care. We are a collaborative, values-driven team that believes in Focus, Discipline, and Accountability. At Tekton Research, we take pride in doing excellent work while fulfilling our mission of Making Life Better.

We offer competitive compensation, comprehensive benefits, and opportunities for professional growth in a supportive and fast-paced research environment.

Position Summary:

The Clinical Research Coordinator (CRC) is responsible for the day-to-day coordination and management of clinical research studies, ensuring compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. The CRC serves as the primary liaison between investigators, sponsors, study participants, and regulatory agencies while ensuring participant safety, data integrity, and successful study execution.

This role requires excellent organizational skills, strong attention to detail, and the ability to manage multiple clinical trials simultaneously in a dynamic environment.

Key Responsibilities:

  • Coordinate and manage all aspects of assigned clinical trials from study start-up through close-out.
  • Recruit, screen, consent, and schedule study participants according to protocol requirements.
  • Collect, process, package, and ship laboratory specimens according to protocol and sponsor requirements.
  • Maintain accurate source documentation, regulatory binders, and study records in compliance with GCP, FDA regulations, and institutional policies.
  • Monitor participant safety and promptly identify, document, and report adverse events.
  • Prepare and submit regulatory documents, including Institutional Review Board (IRB) submissions, continuing reviews, and protocol amendments.
  • Collaborate with investigators, sponsors, monitors, and study staff to ensure successful study conduct.
  • Assist with monitoring visits, sponsor audits, and regulatory inspections.
  • Utilize Electronic Data Capture (EDC) systems and Clinical Trial Management Systems (CTMS) to maintain accurate study data.
  • Ensure protocol compliance while maintaining the highest standards of participant care and research integrity.

Required Qualifications:

  • High school diploma or GED required; Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, or a related field preferred.
  • Minimum of one (1) year of Clinical Research Coordinator experience.
  • Working knowledge of Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and clinical research processes.
  • Experience with pediatric and adult phlebotomy and specimen processing.
  • Strong organizational and time management skills with the ability to prioritize multiple studies.
  • Experience maintaining regulatory documentation and source records.
  • Proficiency with Electronic Data Capture (EDC) systems and Microsoft Office applications.
  • Excellent verbal and written communication skills.
  • Ability to work independently while collaborating effectively with multidisciplinary teams.

Preferred Qualifications:

  • Current ACRP-CRC or SOCRA certification.
  • Advanced degree in Nursing, Public Health, Clinical Research, or a related healthcare field.
  • Experience working on industry-sponsored or multi-center clinical trials.
  • Familiarity with clinical monitoring, participant recruitment, and retention strategies.

Why Join Tekton Research?

At Tekton Research, you'll join a team dedicated to excellence, innovation, and improving lives through clinical research. We foster a collaborative culture where professional development is encouraged, contributions are valued, and every team member plays an important role in advancing healthcare.

If you are passionate about clinical research and committed to providing exceptional patient care, we encourage you to apply and become part of the Tekton Research team.