Top 25 Regulatory affairs Jobs in Shawnee 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
7d
Medical, Legal and Regulatory (MLR) Coordinator
EVERSANA —Overland Park, KS
- Contract
- Remote
- Microsoft Outlook
- Customer service
- Computer literacy
Quick Apply
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
4d
Sr Director, Sci Affairs & Innovation
Hill's Pet Nutrition —Overland Park, KS
- $245,000 - $275,000 a year
- Hybrid work
- 6 years
- Internal Medicine
- Public speaking
- Profit sharing
- Paid parental leave
Medical Editor
EVERSANA —Overland Park, KS
- Contract
- Remote
- Mid-level
- Bachelor's degree
- Doctor of Philosophy
Quick Apply
Senior Regulatory Coordinator - Comprehensive Integrated Research Operations (CIRO)
The University of Kansas Medical Center —Kansas City, MO
- $60,800 - $91,200 a year
- Full-time
- Nursing
- Computer literacy
- Internal Medicine
- Paid jury duty
- Paid holidays
14d
Health System Specialist- Project Management
US Veterans Health Administration —Kansas City, MO
- $108,173 - $140,627 a year
- Online Application
- Background check
- Oracle
- Psychiatry
1d
Lab Coordinator, Chemistry
Johnson County Community College —Overland Park, KS
- $26.94 an hour
- Full-time
- Hybrid work
- Sales
- Word processing
- Computer literacy
- 403(b) matching
- AD&D insurance
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
Manager, Professional Innovation (173105)
Colgate-Palmolive —Overland Park, KS
- $109,600 - $155,000 a year
- Hybrid work
- Doctor of Philosophy
- Travel
- Senior level
- Profit sharing
- Paid parental leave
Senior Clinical Research Coordinator - Cancer Center
The University of Kansas Medical Center —Kansas City, MO
- $70,200 - $105,300 a year
- Full-time
- Computer literacy
- HIPAA
- Master's degree
- Paid jury duty
- Paid holidays
Medical Science Liaison (MSL or Sr. MSL), Neurology (Alzheimer's Disease) - Field Based, Central Midwest (KS, NE, IA & MO)
Eisai —Kansas City, MO
- $144,300 - $216,900 a year
- Weekends as needed
- Clean driving record
- Medicine
- Word processing
Medical Affairs Director
Pegasus Laboratories, Inc. —Shawnee, KS
- PRN
- Background check
- Pass drug screening
- 8 years
- Paid parental leave
- AD&D insurance
Quick Apply
Senior Scientist - Monday-Friday 8AM-5PM
Eurofins USA Clinical Diagnostics —Lenexa, KS
- Full-time
- Background check
- Pass drug screening
- 3 years
- Paid holidays
- Disability insurance
Quick Apply
Clinical Research Physician - Internal Medicine (Part time)
Alcanza Clinical Research —Kansas City, MO
- Part-time
- Spanish
- CPR Certification
- Medicine
- Health savings account
- Disability insurance
Quick Apply
Clinical Research Physician - Dermatologist (Part Time)
Alcanza Clinical Research —Kansas City, MO
- Part-time
- Spanish
- Medicine
- BC/BE
- Health savings account
- Disability insurance
Quick Apply
Clinical Research Nurse Coordinator - Cancer Center
The University of Kansas Medical Center —Kansas City, MO
- $70,200 - $105,300 a year
- Full-time
- Nursing
- RN License
- Bachelor of Science
- Paid jury duty
- Paid holidays
Senior Regulatory Affairs Manager
Argenta —Shawnee, KS
- Full-time
- Remote
- Background check
- Pass drug screening
- 8 years
Quick Apply
Director, Regulatory Affairs – CMC
Rocket Pharmaceuticals —United States
- $204,000 - $264,000 a year
- Full-time
- Bachelor of Science
- 8 years
- Bachelor's degree
- Paid holidays
- Health insurance
Deputy Chief Compliance Officer
Kaztronix —United States
- 11+ years
- Office
- Bachelor's degree
Quick Apply

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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
7 days ago

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

regulatory affairs jobs in shawnee ks

Clinical Research Coordinator - Cancer Center

Medical, Legal and Regulatory (MLR) Coordinator

Regulatory Coordinator - Cancer Center

Sr Director, Sci Affairs & Innovation

Medical Editor

Senior Regulatory Coordinator - Comprehensive Integrated Research Operations (CIRO)

Health System Specialist- Project Management

Lab Coordinator, Chemistry

Clinical Research Coordinator - Internal Medicine (Nephrology)

Manager, Professional Innovation (173105)

Senior Clinical Research Coordinator - Cancer Center

Medical Science Liaison (MSL or Sr. MSL), Neurology (Alzheimer's Disease) - Field Based, Central Midwest (KS, NE, IA & MO)

Medical Affairs Director

Senior Scientist - Monday-Friday 8AM-5PM

Clinical Research Physician - Internal Medicine (Part time)

Clinical Research Physician - Dermatologist (Part Time)

Clinical Research Nurse Coordinator - Cancer Center

Senior Regulatory Affairs Manager

Director, Regulatory Affairs – CMC

Deputy Chief Compliance Officer

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