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Clinical Research Operations Manager Jobs in Kansas

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 ... Coordinate and manage all aspects of assigned clinical trials from study start-up through close-out.

Grene Vision Group

Clinical Research Coordinator

Wichita, KS · 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 ...

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Clinical Research Operations Manager information

See Kansas salary details

$31.2K

$87.4K

$166.3K

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

As of Aug 14, 2026, the average yearly pay for clinical research operations manager in Kansas is $87,436.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,700.00 and $101,200.00 per year, depending on experience, location, and employer.

How does a clinical research operations manager collaborate with cross-functional teams during a study?

As a Clinical Research Operations Manager, you will work closely with cross-functional teams including clinical trial coordinators, data managers, regulatory affairs specialists, and principal investigators. Your role involves facilitating clear communication between departments, ensuring that study milestones are met, and resolving operational issues as they arise. Regular meetings and status updates are common, and you'll often act as a liaison to keep all stakeholders aligned on study objectives, timelines, and compliance requirements. This collaborative approach is crucial for maintaining study integrity and ensuring successful trial outcomes.

What does a clinical research operations manager do?

A Clinical Research Operations Manager oversees the daily operations of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate between research staff, sponsors, and regulatory bodies, manage budgets and timelines, and ensure proper documentation and reporting. Their role is essential in maintaining the quality and integrity of clinical studies from start to finish.

What are the key skills and qualifications needed to thrive as a clinical research operations manager, and why are they important?

To thrive as a Clinical Research Operations Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications such as ACRP or SOCRA are highly valuable. Leadership, problem-solving, and excellent organizational and communication skills help you manage teams and collaborate effectively with stakeholders. These skills and qualities are crucial for ensuring the successful execution of clinical trials while maintaining regulatory standards and operational efficiency.

What are popular job titles related to Clinical Research Operations Manager jobs in Kansas?

For Clinical Research Operations Manager jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Clinical Research Operations Manager jobs in Kansas look for?

The top searched job categories for Clinical Research Operations Manager jobs in Kansas are:

Clinical Research Operations Manager jobs near you
Infographic showing various Clinical Research Operations Manager job openings in Kansas as of August 2026, with employment types broken down into 85% Full Time, 11% Part Time, 1% Temporary, and 3% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $87,436 per year, or $42 per hour.

Regional Director of Clinical Operations

Tekton Research Inc

Wichita, KS • On-site

Full-time

Posted 8 days ago

Job description

Regional Director of Clinical Operations - Oklahoma and Kansas

Position Type: Full-Time | Exempt

Position Summary:

Tekton Research is seeking an experienced Regional Director of Clinical Operations to oversee operational performance, revenue growth, and quality execution across clinical research sites. This strategic leadership role is responsible for ensuring sites achieve key performance indicators (KPIs), meet revenue objectives, maintain compliance with study requirements, and successfully execute clinical trials.

The Regional Director of Clinical Operations serves as a key partner to site leadership, managers, and Principal Investigators (PIs), providing guidance, identifying business risks, implementing solutions, and reporting performance updates to executive leadership.

Reports To: Senior Regional Director of Clinical Operations / Chief Operating Officer (COO)

Essential Responsibilities:
  • Monitor and evaluate study startup performance to support successful trial activation, revenue generation, and future business growth.
  • Assess site revenue performance and provide strategic recommendations to achieve financial goals.
  • Hold sites accountable for appropriate scheduling, recruitment strategies, and operational execution to meet or exceed recruitment and revenue targets.
  • Provide oversight to ensure sites are appropriately staffed, trained, and prepared to meet study conduct requirements.
  • Ensure sites maintain appropriate resources, equipment, and operational readiness for successful study execution.
  • Monitor site compliance with contractual requirements, including completion of study visits, EDC entry, query resolution, and required documentation.
  • Serve as a clinical research resource to support sites with operational and study-related questions.
  • Ensure sites are conducting quality control activities and partner with Quality Assurance (QA) as needed for audits, inspections, and quality initiatives.
  • Collaborate with site managers and Principal Investigators to ensure appropriate investigator coverage and study support.
  • Communicate site goals, expectations, and performance metrics with managers and investigators.
  • Track and report site performance, progress, challenges, and business risks to the Executive Director and/or COO.
  • Develop and implement solutions to mitigate operational and business risks.
  • Perform other duties as assigned.
Required Knowledge, Skills, and Abilities:

Successful candidates will have demonstrated expertise in:

  • Clinical research operations and study management
  • Regulatory requirements and compliance
  • Clinical procedures and trial execution
  • Sponsor communication and relationship management
  • Project management principles
  • Human resources and team leadership practices
  • Operational performance management and KPI oversight
Education and Experience:
  • Bachelor’s degree, specialized degree, or equivalent relevant education and experience preferred.
  • 7–10 years of experience in the clinical research industry.
  • 5+ years of experience in a supervisory or management leadership role.
  • Proven experience managing clinical research operations, site performance, and cross-functional teams.
Physical Requirements:
  • Ability to work extended periods at a desk and on a computer.
  • Ability to occasionally lift up to 15 pounds.
  • Willingness and ability to travel, including air travel, to support sites within the Oklahoma and Kansas region.
Why Join Tekton Research?

At Tekton Research, we are committed to advancing clinical research through operational excellence, quality patient care, and strong partnerships with sponsors, investigators, and research teams. The Regional Director of Clinical Operations plays a critical role in driving site success and supporting the delivery of high-quality clinical trials.