Top 187 Clinical data coordinator Jobs in Kansas

Clinical Research Coordinator - Wichita, KS
IQVIA —Wichita, KS
- $35 - $42 an hour
- Part-time
- Vital signs
- Office
- Bachelor's degree
Clinical Research Coordinator II
U.S. Dermatology Partners —Leawood, KS
- $65,000 - $75,000 a year
- Full-time
- Microsoft Outlook
- OSHA
- Patient monitoring
Quick Apply
1d
Registered Nurse Medical ICU
Ascension —Wichita, KS
- Full-time
- Nursing
- Patient monitoring
- RN License
- Disability insurance
- Health insurance
Registered Nurse - Clinical Research Coordinator- RN
Wichita Urology Group —Wichita, KS
- Full-time
- Nursing
- RN License
- Laboratory experience
- Health savings account
- Health insurance
Quick Apply
Phlebotomist
University of Kansas Health System —Kansas City, KS
- Full-time
- Hospital
- English
- High school diploma or GED
MDS Coordinator | RN
The Village at Mission —Prairie Village, KS
- $85,000 - $90,000 a year
- RN License
- Mid-level
- In-person
- Paid holidays
- Health insurance
Registered Nurse Team Director (RN)
Moments Hospice —Wichita, KS
- $90,000 - $100,000 a year
- Full-time
- Nursing
- RN License
- Mid-level
- Dental insurance
- Paid time off
Quick Apply
4d
Credentialing Lead - Onsite
ProviDRs Care —Wichita, KS
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Office
- Health savings account
- Health insurance
Quick Apply
Clinical Research Coordinator
INNOVO RESEARCH INC —Hutchinson, KS
- Weekends as needed
- Writing skills
- English
- Mid-level
- Disability insurance
- Health insurance
Quick Apply
Patient Intake Coordinator
Clear Choice —Overland Park, KS
- $22 - $24 an hour
- Full-time
- Dental office
- Computer literacy
- Office
- Paid holidays
- Health insurance
7d
Assessment Coordinator
Cottonwood Springs —Olathe, KS
- Overtime
- Vital signs
- Hospital
- Mid-level
- Disability insurance
- Health insurance
Quick Apply
Coordinator II - Ambulatory
The University of Kansas Health System —Kansas City, KS
- Full-time
- Mid-level
- Office
- Supervising experience
Behavioral Health Intake Coordinator (Evenings)
The University of Kansas Health System —Overland Park, KS
- Full-time
- Hospital
- Customer service
- Inpatient
Health Information Coordinator/Scheduler
St. Croix Hospice —Atchison, KS
- Full-time
- Clean driving record
- Computer literacy
- Pass drug screening
Quick Apply
Health Care Data Analyst
State of Kansas - Dept of Health & Environment —Shawnee County, KS
- $26.50 - $28.84 an hour
- Full-time
- Mid-level
- High school diploma or GED
- Analysis skills
- Paid holidays
- Health insurance
4d
Clinical Research Coordinator
Grene Vision Group —Wichita, KS
- Background check
- Anatomy knowledge
- Microsoft Outlook
- Paid parental leave
- Paid holidays
Quick Apply
4d
Security Identification Coordinator
The University of Kansas Health System —Kansas City, KS
- Full-time
- Hospital
- Word processing
- Mid-level
RN Quality & Outcomes Coordinator
AdventHealth Shawnee Mission —Shawnee Mission, KS
- $67,600 - $125,736 a year
- Full-time
- CPR Certification
- Nursing
- RN License
- Paid parental leave
- Disability insurance
Surgical Patient Coordinator
Thrive Reconstructive Surgery —Wichita, KS
- $48,000 - $55,000 a year
- Weekends as needed
- Surgery
- Medical office experience
- HIPAA
- Paid training
- Health insurance
Quick Apply
11d
PAI Assistant
Lifepoint Rehabilitation —Kansas
- 8 hour shift
- Acute care
- Hospital
- Inpatient
- Tuition reimbursement
- 401(k) matching
Quick Apply

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Clinical Research Coordinator - Wichita, KS

IQVIA -
Wichita, KS

Apply Now

Job Details

Part-time
$35 - $42 an hour

Qualifications

Employee relationship building

Full Job Description

Wichita, United States of America | Part time | Office-based | R1550059

Clinical Research Coordinator – Wichita, KS
Work Set-Up: On-site
Schedule: Part-time, 24 hours per week

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. By combining deep scientific expertise with advanced technology, we deliver high-quality insights and support that help shape the future of clinical research.

About the Role

IQVIA is seeking a Clinical Research Coordinator (CRC) to support the successful execution of clinical research studies under the guidance of the Principal Investigator. This role is ideal for candidates with hands-on clinical research experience who are passionate about patient care, data quality, and advancing healthcare innovation.

The CRC will play a critical role in study coordination, patient engagement, clinical procedures, and data management while ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

Key Responsibilities

Perform clinical procedures including ECGs, vital signs, specimen/sample collection, and other protocol-required activities.
Coordinate and support daily clinical trial activities in compliance with study protocols, GCP, and site procedures.
Conduct patient chart reviews and prescreening activities to identify potentially eligible participants.
Recruit, screen, schedule, and orient study participants while ensuring patient safety and a positive participant experience.
Support patient visits and assist with study-related documentation and follow-up activities.
Prepare study materials, maintain study supplies, and assist with equipment setup and logistical planning.
Collect, review, and accurately document clinical data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems.
Support EDC data entry, query resolution, and data quality review in collaboration with investigators, sponsors, and monitors.
Respond to sponsor and monitor queries in a timely and accurate manner.
Maintain confidentiality, regulatory compliance, and adherence to Health & Safety policies.
Act as a patient advocate and contribute to a collaborative and professional research environment.

Qualifications

Bachelor’s degree preferred, or an equivalent combination of education and relevant experience.
Minimum of 1+ years of relevant clinical research experience.
Working knowledge of clinical trials, GCP guidelines, and medical terminology.
Experience with patient chart review and prescreening activities.
Ability to support patient visits and study coordination activities in a clinical research environment.
Experience with EDC systems, including data entry and query resolution.
Strong attention to detail with excellent organizational and communication skills.
Ability to build effective working relationships with patients, investigators, sponsors, and team members.

Please Note

This position is not eligible for sponsorship.

#LI-CES #LI-DNP #LI-HCP #ONSITE

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Where you'll work

Office-based

You’ll work primarily from one of our office locations, collaborating closely with colleagues in a dynamic, team-oriented environment. This setting offers access to on-site resources, real-time interaction and opportunities to build strong relationships through in-person work.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

clinical data coordinator jobs in kansas

Clinical Research Coordinator - Wichita, KS

Clinical Research Coordinator II

Registered Nurse Medical ICU

Registered Nurse - Clinical Research Coordinator- RN

Phlebotomist

MDS Coordinator | RN

Registered Nurse Team Director (RN)

Credentialing Lead - Onsite

Clinical Research Coordinator

Patient Intake Coordinator

Assessment Coordinator

Coordinator II - Ambulatory

Behavioral Health Intake Coordinator (Evenings)

Health Information Coordinator/Scheduler

Health Care Data Analyst

Clinical Research Coordinator

Security Identification Coordinator

RN Quality & Outcomes Coordinator

Surgical Patient Coordinator

PAI Assistant

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Clinical Research Coordinator – Wichita, KS
Work Set-Up: On-site
Schedule: Part-time, 24 hours per week

#LI-CES #LI-DNP #LI-HCP #ONSITE

Where you'll work

Office-based

Culture

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clinical data coordinator jobs in kansas

I want to receive the latest job alert for clinical data coordinator in kansas

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Clinical Research Coordinator – Wichita, KS Work Set-Up: On-site Schedule: Part-time, 24 hours per week

#LI-CES #LI-DNP #LI-HCP #ONSITE

Where you'll work

Office-based

Culture

Clinical Research Coordinator – Wichita, KS
Work Set-Up: On-site
Schedule: Part-time, 24 hours per week