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Clinical Research Operations Manager Jobs in Kansas

Iterative Health

Research Assistant - Wichita, KS

Wichita, KS · On-site

$17.25 - $23.75/hr

... site management to support the day-to-day conduct of active clinical trials. This role assists ... Prior clinical research experience or exposure to clinical trial operations. * Familiarity with GCP ...

Argenta

Manager of Clinical Operations

Shawnee, KS · Hybrid

Recommends, develops, andregularlyfacilitatesinnovative learning for Clinical Research Associatesof ... clinical operations management * A collaborative working style to be able to lead and motivate ...

Argenta

Manager of Clinical Operations

Shawnee, KS · On-site

Recommends, develops, and regularly facilitates innovative learning for Clinical Research ... clinical operations management * A collaborative working style to be able to lead and motivate ...

Medix

Clinical Research Nurse

Overland Park, KS · On-site

$38 - $42/hr

Administer clinical trials in accordance with research protocols. * Monitor patient health and ... Due to these job duties, this position has a significant impact on the business operations and ...

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All JobsClinical Research Operations JobsClinical Research Operations Manager JobsClinical Research Operations Manager Jobs in Kansas

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 Sep 5, 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.

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.

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 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 86% Full Time, 12% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $87,436 per year, or $42 per hour.

Clinical Research Coordinator

Professional Case Management

Kansas City, KS • On-site

$23.50 - $31/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 6 days ago

Professional Case Management rating

5.0

Company rating: 5.0 out of 10

Based on 10 frontline employees who took The Breakroom Quiz

Job description

Put your talents to work at PCM! Whether you work in our Home Care, Clinical Research, Impairments, or Catastrophic Care division, you will support our mission to deliver care and other services that enhance the quality of life of our clients. Be a part of our dynamic client-focused team and make a difference in your career!

As an on-site Clinical Research Coordinator (CRC), you will provide technical and administrative support to your assigned clinical operations team in the field as well as direct patient care of research study participants. You work with a high attention to detail, reviewing documentation, coordinating clinical study project details, and maintaining data systems - all with a sense of urgency aligned with that of our customers. The position will involve the conduct of trial coordinator activities for EmVenio Research' decentralized network. This will include assessing and following trial participants along with other trial protocol-related activities. In this role the CRC is accountable for the regulatory compliance and performance of assigned mobile clinics and clinician teams conducting decentralized trials as well as patient engagement, and screening. Additional focus will be on timely and accurate EDC data entry and query resolution.

QUALIFICATIONS

  • Bachelor's degree (B. A. / B. S.) from four-year college or university or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities
  • Two (2) years research experience strongly preferred. Phlebotomy and ECGs experience not required, but preferred.
  • ACRP or SOCRA Clinical Research Certification (Preferred), Clinical Research Training Certification (Preferred)
  • Excellent computer skills, proficient in MS Word, Excel, PowerPoint and ability to obtain knowledge and master all clinical trial database systems.
  • Proven ability to successfully coordinate multiple studies adhering to regulatory and institutional guidelines.

  • Proven ability to communicate effectively within an interdisciplinary team to ensure safe, efficient, quality patient care, both in-person and virtually.

  • Excellent organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively.

  • Ability to effectively analyze project specific data/systems to ensure accuracy and efficiency.

  • Flexibility to reprioritize workload to meet changing project timelines.

  • Responsible for adhering to FDA Good Clinical Practices, FDA regulations, EmVenio Research/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout.

  • Ability to successfully complete EmVenio Research clinical training program.

  • Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

  • Must have strong interpersonal skills to be able to interact with multiple people on many different levels.

  • May be responsible for basic clinical assessments.

ESSENTIAL FUNCTIONS/AREAS OF ACCOUNTABILITY

  • Complete study tasks as outlined by trial protocol

  • Ensures documentation is accurate according to EmVenio guidelines and protocols is required

  • Achieves EmVenio standards for quality, customer service, productivity and teamwork through participation in Risk and Quality Improvement programs, clinical meetings and other meetings as required

  • Works collaboratively with nurses, physicians, nurse practitioners, physician assistants, clinical research specialists, leaders, family members, key care givers and any ancillary medical personnel as appropriate

  • Communicates with key stakeholders such as the Principal Investigator, clinical trials team and quality department, regulatory

  • Certain assignments may require provider to perform ECGs, draw blood (Phlebotomy), process and ship lab specimen, etc.

  • Consults with the Site Manager and virtual Clinical Research Coordinator to ensure compliance with guidelines

  • Reviews the medical and social history of members

  • Assist in building the community research site network and developing relationships within that community

  • Participates in recruitment of participants to include personally engaging the general public face to face in local across hard-to-reach communities, attending community events, speaking with physicians and people across diverse cultures and backgrounds to support meeting participant enrollment targets

  • Documenting recruiting efforts and outreach progress

  • Facilitates conversations with potential participants through both inbound and outbound calls sometimes serving as their first introduction to research

  • Participates in all mandatory compliance, patient engagement and other training programs, seeks guidance for compliance-related concerns and adheres to all applicable laws, regulations and EmVenio policies and procedures

  • Maintains positive control of all PHI information

  • Participates in required training and education programs

  • Ensures adherence to clinical trial protocols and supports the clinical trials team in ensuring that trials are conducted and comply with all regulatory, state, national and internationally accepted guidelines for Good Clinical Practice (ICH GCP).

  • Ensures timely and accurate data collection and completion of case report forms relevant to clinical trials or research projects.

  • Assists in liaising with monitors of clinical trials and available to monitor and/or audit when required, with full patient documentation available.

  • Assists in educating EmVenio Research staff and participants regarding the designated clinical trial and procedures and relevant investigations associated with the designated clinical trial and to raise the profile of research throughout the EmVenio Research.

  • Any other duties needed to help drive EmVenio's purpose, fulfill our mission, and abide by our core values.

The typical base pay range for this role is USD $56,160 - $76,960 per year.

Individual base pay depends on various factors, in addition to primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience, skills and other market-based factors.

Available Benefits Include

  • Medical
  • Dental
  • Vision
  • 401(k)
  • Company Paid Short Term Disability
  • Flexible Spending Account (FSA)
  • Health Savings Account (HSA)
  • Paid Time Off
  • Voluntary Benefits
Please contact Carson Moreira-Rego at (866) 776-0127 x387 or at Carson.Moreira-Rego@procasemanagement.com today to learn more about our opportunities where you can make a difference in your own career!

Professional Case Management is an Equal Opportunity Employer.

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About Professional Case Management

Sourced by ZipRecruiter

Since 1997, Professional Case Management (PCM) has been providing quality, nationwide in-home nursing services to sufferers of chronic diseases. We are the nation's premier healthcare provider for nuclear weapons workers, uranium miners, millers and haulers suffering from illnesses contracted in the course of their employment. Our mission is to deliver quality care to enhance patient outcomes in the privacy and comfort of their homes.

Industry

Health care and social assistance

Company size

201 - 500 Employees

Headquarters location

Denver, CO, US

Year founded

1986

Social media

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