Top 53 Clinical research associate Jobs in Overland Park Ks

Clinical Research Coordinator - Cancer Center
University of Kansas Medical Center —Kansas City, KS
- $60,800 - $91,200 a year
- Online Application
- HIPAA
- Mid-level
- Microsoft Office
- Paid jury duty
- Paid parental leave
Laboratory Coordinator (Correlative Lab) Cancer Center
University of Kansas Medical Center —Kansas City, KS
- $22.26 - $31.15 an hour
- Online Application
- Microsoft Outlook
- Computer literacy
- HIPAA
- Paid jury duty
- Paid parental leave
4d
Clinical Research Assistant - Cancer Center
The University of Kansas Medical Center —Kansas City, MO
- $22.88 - $33.17 an hour
- Full-time
- Nursing
- Computer literacy
- Bachelor's degree
- Paid jury duty
- Paid holidays
Clinical Research Coordinator
Kansas City Card Arrhythmia Research —Overland Park, KS
- Full-time
- Mid-level
- In-person
- Cardiology
- Employee stock purchase plan
- Disability insurance
Quick Apply
9d
Clinical Research Coordinator
EmVenio Research —Kansas City, KS
- $56,160 - $76,960 a year
- Full-time
- Microsoft Word
- Bachelor of Science
- Mid-level
- Health savings account
- Disability insurance
Quick Apply
12d
Clinical Research Coordinator - Internal Medicine (All of Us)
The University of Kansas Medical Center —Kansas City, MO
- $60,800 - $91,200 a year
- Weekends as needed
- Computer literacy
- Writing skills
- Internal Medicine
- Paid jury duty
- Paid holidays
7d
Clinical Research Coordinator - Pediatrics
The University of Kansas Medical Center —Kansas City, MO
- $60,800 - $91,200 a year
- Full-time
- HIPAA
- Mid-level
- University
- Paid jury duty
- Paid holidays
Site Research Assistant - Kansas City, MO
IQVIA —Kansas City, MO
- $25 - $39 an hour
- Part-time
- Office
- Experience equivalent to degree accepted
- 1 year
Clinical Research Coordinator - Internal Medicine (Nephrology)
The University of Kansas Medical Center —Kansas City, MO
- $60,800 - $91,200 a year
- Full-time
- Internal Medicine
- HIPAA
- Mid-level
- Paid jury duty
- Paid holidays
Clinical Research Coordinator - Women's Health Department
University Health KC —Kansas City, MO
- Full-time
- Hospital
- Computer literacy
- HIPAA
Senior Clinical Research Associate, Sponsor Dedicated
IQVIA —Overland Park, KS
- $74,500 - $197,500 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Clinical Research Coordinator, On-Site
IQVIA —Kansas City, MO
- $37,800 - $94,500 a year
- Full-time
- Patient monitoring
- Mid-level
- Office
CRA 1, IQVIA Biotech
IQVIA —Overland Park, KS
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
Data And Research Specialist
The University of Kansas Health System —Westwood, KS
- Full-time
- Mid-level
- High school diploma or GED
- Computer skills
Clinical Research Assistant II
Children's Mercy KC —Kansas City, MO
- From $24.14 an hour
- Full-time
- Pass drug screening
- Mid-level
- 3 years
Clinical Research Technician
DR VINCE CLINICAL RESEARCH PA —Overland Park, KS
- BLS Certification
- High school diploma or GED
- 1 year
Quick Apply
6d
Regulatory Coordinator - Cancer Center
The University of Kansas Medical Center —Kansas City, MO
- $28.20 - $38.35 an hour
- Full-time
- Nursing
- Microsoft Excel
- Microsoft Outlook
- Paid jury duty
- Paid holidays
Clinical Research Assistant - Internal Medicine (Physical Activity and Weight Management)
The University of Kansas Medical Center —Kansas City, MO
- $22.88 - $33.17 an hour
- Full-time
- Internal Medicine
- Mid-level
- Master's degree
- Paid jury duty
- Paid holidays
Phlebotomist - Clinical Research Technician II
Altasciences —Overland Park, KS
- Full-time
- Customer service
- English
- Mid-level
- Paid holidays
- Health insurance
Senior Clinical Research Associate, Sponsor Aligned, Oncology
IQVIA —Overland Park, KS
- $71,900 - $189,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree

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Clinical Research Coordinator - Cancer Center

University of Kansas Medical Center -
Kansas City, KS

Apply Now

Job Details

Full-time
$60,800 - $91,200 a year

Benefits

Paid jury duty
Paid parental leave
Paid holidays
Disability insurance
Health insurance
Dental insurance
Paid time off
Parental leave
Vision insurance
403(b)
Life insurance

Qualifications

HIPAA compliance
HIPAA
Project coordination
Microsoft Office
Research regulatory compliance
Data collection

Full Job Description

Clinical Research Coordinator - Cancer Center

Department:
SOM KC Cancer Center Clinical Trials
-
Clinical Research

Position Title:
Clinical Research Coordinator - Cancer Center

Job Family Group:
Professional Staff

Job Description Summary:
The Clinical Research Coordinator works collaboratively with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research. 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. Monitors participants' progress including documenting and reporting adverse events. Participates in periodic quality assurance audits of protocols.

The University of Kansas Cancer Center is the only National Cancer Institute designated Comprehensive Cancer Center in the region, 1 of only 57 in the nation to receive this distinction. Patients gain access to the most promising therapies, cutting-edge clinical trials and world class research.

Job Description:

Job Responsibilities

Under the direction of the principal investigator, recruit and educate potential patients for and evaluate potential patient eligibility for clinical trials.
Maintain source documents and submit case report forms (CRFs) as required for clinical trials.
Recognize and report adverse events/serious adverse events to the Principal Investigator, FDA, and sponsors.
Perform study procedures, as outlined in the protocol and within state and institutional scope of practice.
Assist clinical staff with phlebotomy and sample collection, processing, handling, and shipping as outlined in the protocol and within institutional/KUMC policy.
Ensure adequate study supplies are being maintained. Track study expenditures and submit reimbursement requests for study equipment, supplies and study participants.
Prepare documentation and participate in study monitoring visits, reviews and audits. Provide written and verbal reports to Principal Investigator and Project Manager, as required.
Participate in quality assurance activities by reviewing clinical data in medical record charts, assessing pharmacy compliance with protocol criteria and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR.
Work closely with the Research Institute and Human Research Protection Program and have a working knowledge of KUMC policies and procedures.
Attend continuing education, research and training seminars as requested by manager.

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible job responsibilities, tasks, duties, and assignments. Furthermore, job duties, responsibilities and activities may change at any time with or without notice.

Work Environment: This position will be 100% onsite due to the fact this is a patient facing role.

Required Qualifications

Work Experience:

4 years of relevant work experience. Education may be substituted for experience on a year for year basis.
Experience with regulations governing clinical research (CFR, GCP, HIPAA).
Experience with statutes and guidelines relevant to regulatory affairs in clinical research.
Experience using MS Office products.

Preferred Qualifications

Education: Bachelor's degree.

Work Experience:

Experience study budgets, contracts, and grant applications.

Certifications/Licenses:

Certified Clinical Research Coordinator (CCRC)
Certified Clinical Research Professional (CCRP)

Skills

Attention to detail
Time Management
Interpersonal Skills
Communication.
Organization.
Multi-tasking.

Required Documents

Resume
Cover Letter

Comprehensive Benefits Package:

Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html

Employee Type:
Regular

Time Type:
Full time

Rate Type:
Salary

Compensation Statement:

The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above.

Pay Range:
$60,800.00 - $91,200.00
Minimum
$60,800.00
Midpoint
$76,000.00
Maximum
$91,200.00

Application Instructions:
To learn more and apply online, please visit https://kumc.wd5.myworkdayjobs.com/en-US/kumc-jobs/job/Kansas-City-Metro-Area/Clinical-Research-Coordinator-Cancer-Center_JR009760 or go to https://careers.kumc.edu/ and search for position number JR009760.

Applications must be submitted directly through the KU Medical Center website to be considered for this position. Any applications submitted via email or this website will NOT be reviewed or considered.

About KU Medical Center:
The University of Kansas Medical Center's mission is to educate exceptional health care professionals through a full range of undergraduate, graduate, professional, postdoctoral and continuing education programs in the schools of Medicine, Nursing and Health Professions. KU Medical Center also advances the health sciences through world-class research programs; provides compassionate and state-of-the-art patient care in an academic medical center environment; and works with communities in every Kansas county to improve the health of Kansans. Learn more at www.kumc.edu.

Benefits:
KUMC offers a range of great benefits that support employees and eligible family members. Our health insurance benefits begin on hire date and KUMC offers other exciting benefits such as paid parental leave, generous employer retirement contributions and other resources to improve health and well-being. For more information, please visit https://www.kumc.edu/human-resources/benefits.html

Equal Employment Opportunity Statement

The University of Kansas Medical Center is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, national origin, ethnicity, ancestry, age, protected veteran or disability status, marital status, parental status, or genetic information. http://policy.ku.edu/IOA/nondiscrimination">http://policy.ku.edu/IOA/nondiscrimination

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Refine Your Search

clinical research associate jobs in overland park ks

Clinical Research Coordinator - Cancer Center

Laboratory Coordinator (Correlative Lab) Cancer Center

Clinical Research Assistant - Cancer Center

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator - Internal Medicine (All of Us)

Clinical Research Coordinator - Pediatrics

Site Research Assistant - Kansas City, MO

Clinical Research Coordinator - Internal Medicine (Nephrology)

Clinical Research Coordinator - Women's Health Department

Senior Clinical Research Associate, Sponsor Dedicated

Clinical Research Coordinator, On-Site

CRA 1, IQVIA Biotech

Data And Research Specialist

Clinical Research Assistant II

Clinical Research Technician

Regulatory Coordinator - Cancer Center

Clinical Research Assistant - Internal Medicine (Physical Activity and Weight Management)

Phlebotomist - Clinical Research Technician II

Senior Clinical Research Associate, Sponsor Aligned, Oncology

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