1

Manager Clinical Research Informatics Jobs in Wichita, KS

Clinical Research Coordinator

Wichita, KS ยท On-site

$21.50 - $28.75/hr

Clinical Research Coordinator (CRC) About Tekton Research: Tekton Research is a growth-oriented ... Coordinate and manage all aspects of assigned clinical trials from study start-up through close-out.

Clinical Research Coordinator

Wichita, KS ยท On-site

$21.75 - $28.75/hr

Employee Discounts JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily operations of clinical trials. Duties ...

The ideal candidate will be someone who can manage multiple concurrent projects, provide strong ... Experience mentoring clinical faculty in research or scholarly activity * Experience with IRB ...

On-Site Manager

Wichita, KS ยท On-site

$43.27 - $57.69/hr

Job Summary Our client is seeking a dynamic On-Site Manager to lead the operational success, clinical quality, and growth of two local research clinics. The role includes managing day-to-day ...

next page

Showing results 1-20

Manager Clinical Research Informatics information

See Wichita, KS salary details

$43.8K

$96K

$169.1K

How much do manager clinical research informatics jobs pay per year?

As of Aug 10, 2026, the average yearly pay for manager clinical research informatics in Wichita, KS is $96,023.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,500.00 and $109,600.00 per year, depending on experience, location, and employer.
What are popular job titles related to Manager Clinical Research Informatics jobs in Wichita, KS? For Manager Clinical Research Informatics jobs in Wichita, KS, the most frequently searched job titles are:
What job categories do people searching Manager Clinical Research Informatics jobs in Wichita, KS look for? The top searched job categories for Manager Clinical Research Informatics jobs in Wichita, KS are:
Infographic showing various Manager Clinical Research Informatics job openings in Wichita, KS as of June 2026, with employment types broken down into 1% As Needed, 88% Full Time, 8% Part Time, 2% Temporary, and 1% Contract. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $96,023 per year, or $46.2 per hour.

Clinical Research Coordinator

Tekton Research Inc

Wichita, KS โ€ข On-site

$21.50 - $28.75/hr

Full-time

Posted 9 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.