About The Role The Clinical Research Nurse II will oversee the safety and consent of clinical trial ... Other tasks as assigned by management What You'll Need to Succeed Education: Degree from accredited ...
About The Role The Clinical Research Nurse II will oversee the safety and consent of clinical trial ... Other tasks as assigned by management What You'll Need to Succeed Education: Degree from accredited ...
Clinical Research Coordinator - Cancer Center
Kansas City, KS · On-site
$23.50 - $31/hr
This position manages assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data.
Clinical Research Coordinator - Cancer Center
Kansas City, KS · On-site
$23.50 - $31/hr
This position manages assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data.
Proven ability to manage priorities and drive study quality independently * Experience mentoring or ... Passion for advancing clinical research and improving patient outcomes When you join ICON Strategic ...
Proven ability to manage priorities and drive study quality independently * Experience mentoring or ... Passion for advancing clinical research and improving patient outcomes When you join ICON Strategic ...
About The Role The Clinical Research Nurse II will oversee the safety and consent of clinical trial ... Other tasks as assigned by management What You'll Need to Succeed Education: Degree from accredited ...
About The Role The Clinical Research Nurse II will oversee the safety and consent of clinical trial ... Other tasks as assigned by management What You'll Need to Succeed Education: Degree from accredited ...
... management. Paramedic candidates without research experience are encouraged to apply. Key ... Research & Operational Responsibilities * Assist in planning, coordinating, and executing clinical ...
Quick apply
... management. Paramedic candidates without research experience are encouraged to apply. Key ... Research & Operational Responsibilities * Assist in planning, coordinating, and executing clinical ...
Senior Clinical Research Coordinator - Cancer Center
Kansas City, KS · On-site
$23.50 - $31/hr
The Senior Clinical Research Coordinator will manage assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and ...
Senior Clinical Research Coordinator - Cancer Center
Kansas City, KS · On-site
$23.50 - $31/hr
The Senior Clinical Research Coordinator will manage assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and ...
... management. Paramedic candidates without research experience are encouraged to apply. Key ... Research & Operational Responsibilities * Assist in planning, coordinating, and executing clinical ...
Quick apply
... management. Paramedic candidates without research experience are encouraged to apply. Key ... Research & Operational Responsibilities * Assist in planning, coordinating, and executing clinical ...
... management. Paramedic candidates without research experience are encouraged to apply. Key ... Research & Operational Responsibilities * Assist in planning, coordinating, and executing clinical ...
... management. Paramedic candidates without research experience are encouraged to apply. Key ... Research & Operational Responsibilities * Assist in planning, coordinating, and executing clinical ...
Senior Clinical Research Coordinator - Cancer Center
Kansas City, KS · On-site
$23.50 - $31/hr
The Senior Clinical Research Coordinator will manage assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and ...
Senior Clinical Research Coordinator - Cancer Center
Kansas City, KS · On-site
$23.50 - $31/hr
The Senior Clinical Research Coordinator will manage assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and ...
... management. Paramedic candidates without research experience are encouraged to apply. Key ... Research & Operational Responsibilities * Assist in planning, coordinating, and executing clinical ...
... management. Paramedic candidates without research experience are encouraged to apply. Key ... Research & Operational Responsibilities * Assist in planning, coordinating, and executing clinical ...
The Clinical Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation and ...
The Clinical Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation and ...
Clinical Research Coordinator / Registered Nurse
Topeka, KS · On-site
$65K - $81K/yr
The Clinical Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation and ...
Clinical Research Coordinator / Registered Nurse
Topeka, KS · On-site
$65K - $81K/yr
The Clinical Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation and ...
Clinical Research Coordinator - Internal Medicine (Nephrology)
Kansas City, KS · On-site
$60.80 - $91.20/hr
This position oversees assigned studies, managing complex activities related to the collection, documentation, and analysis of clinical research data. Additionally, the Clinical Research Coordinator ...
Clinical Research Coordinator - Internal Medicine (Nephrology)
Kansas City, KS · On-site
$60.80 - $91.20/hr
This position oversees assigned studies, managing complex activities related to the collection, documentation, and analysis of clinical research data. Additionally, the Clinical Research Coordinator ...
About The Role The Clinical Research Nurse II will oversee the safety and consent of clinical trial ... Other tasks as assigned by management What You'll Need to Succeed Education: Degree from accredited ...
About The Role The Clinical Research Nurse II will oversee the safety and consent of clinical trial ... Other tasks as assigned by management What You'll Need to Succeed Education: Degree from accredited ...
... manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical ... research and study protocols · Screens and recruits patients based on protocol criteria · ...
New
... manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical ... research and study protocols · Screens and recruits patients based on protocol criteria · ...
New
... manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical ... research and study protocols · Screens and recruits patients based on protocol criteria · ...
New
... manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical ... research and study protocols · Screens and recruits patients based on protocol criteria · ...
New
... manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical ... research and study protocols · Screens and recruits patients based on protocol criteria · ...
New
... manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical ... research and study protocols · Screens and recruits patients based on protocol criteria · ...
New
About The Role The Clinical Research Nurse II will oversee the safety and consent of clinical trial ... Capable of managing multiple conflicting priorities. * Relevant industry experience a plus. Work ...
About The Role The Clinical Research Nurse II will oversee the safety and consent of clinical trial ... Capable of managing multiple conflicting priorities. * Relevant industry experience a plus. Work ...
... manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical ... research and study protocols · Screens and recruits patients based on protocol criteria · ...
... manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical ... research and study protocols · Screens and recruits patients based on protocol criteria · ...
Clinical Research Coordinator - Internal Medicine (Nephrology)
Kansas City, KS · On-site
$23.50 - $31/hr
This position oversees assigned studies, managing complex activities related to the collection, documentation, and analysis of clinical research data. Additionally, the Clinical Research Coordinator ...
Clinical Research Coordinator - Internal Medicine (Nephrology)
Kansas City, KS · On-site
$23.50 - $31/hr
This position oversees assigned studies, managing complex activities related to the collection, documentation, and analysis of clinical research data. Additionally, the Clinical Research Coordinator ...
Clinical Research Operations Manager information
See Kansas salary details
$31.2K - $43.5K
5% of jobs
$43.5K - $55.8K
8% of jobs
$63.5K is the 25th percentile. Wages below this are outliers.
$55.8K - $68.1K
18% of jobs
The median wage is $79.4K / yr.
$68.1K - $80.3K
20% of jobs
$80.3K - $92.6K
19% of jobs
$96.6K is the 75th percentile. Wages above this are outliers.
$92.6K - $104.9K
14% of jobs
$104.9K - $117.2K
8% of jobs
$117.2K - $129.5K
3% of jobs
$129.5K - $141.8K
1% of jobs
$141.8K - $154K
2% of jobs
$154K - $166.3K
1% of jobs
$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:
- Virtual Research Assistant
- Clinical Research Site Manager
- Sr Clinical Research Coordinator
- Per Diem Clinical Research
- Senior Clinical Research Associate
- Remote Clinical Research Dental
- Clinical Trial Research Coordinator
- Manager Ucsf Clinical Research
- Dermatology Clinical Research Remote
- Contract Clinical Trial Manager
Altasciences rating
7.6
Based on 17 frontline employees who took The Breakroom Quiz
61st of 121 rated laboratories
Job description
About The Role
The Clinical Research Nurse II will oversee the safety and consent of clinical trial participants during study conduct and the maintenance of safety equipment. The Clinical Research Nurse II will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).
Work Schedule:Evenings/Overnight
What You'll Do Here
Perform scheduled inspection of emergency crash carts, inventory/inspect the contents, and maintain up to date records.
May train employees on clinical trial activities associated to their job's needs.
Ensure the confidentiality of clinical trial participants and sponsors is respected.
Perform clinical trial activities including but not limited to, continuous safety monitoring, safety assessments, Investigational Product (IP) administration and catheter installation.
Monitor, document and/or follow-up on participant adverse events.
Maintain and advocate a high level of patient care, quality, and safety within the department.
May assist in study related consenting with participant screenings.
Provide feedback, where necessary, to appropriate team members of study progress.
Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
Other tasks as assigned by management
What You'll Need to Succeed
Education:
Degree from accredited Registered Nurse program required or bachelor's degree in nursing from an accredited school.
Work Experience:
Minimum of 4+ years of related clinical research experience required.
Certificates/Licenses /Registrations:
US requirements:
Current Registered Nurse (RN) license, required
Current Basic Life Support (BLS, CPR/AED) certification, required
Current Advanced Cardiac Life Support (ACLS) certification, required
Canadian requirements:
Ordre des infirmieres et infirmiers du Quebec (OIIQ) permit
Cardiopulmonary resuscitation (CPR) certification, required.
Advanced Cardiovascular Life Support (ACLS) certifications, required
Technical Skills:
Microsoft suite
Strong computer literacy
Language(s) Skills:
- Ability to read and interpret technical documents and industry specific manuals.
- Ability to write advanced reports and correspondence.
- Ability to speak effectively before groups of customers or employees of the organization.
- Bilingual proficiency in French may be required, depending on location.
Other Requirements:
- Excellent verbal and written communication skills.
- Well-developed interpersonal skills are required.
- Personal/professional integrity and proven discretion in handling confidential information.
- Capable of managing multiple conflicting priorities.
- Relevant industry experience a plus.
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What Altasciences employees say
Pay
Benefits
Hours and flexibility
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About Altasciences
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
1,001 - 5,000 Employees
Headquarters location
Overland Park, KS, US