Top 48 Clinical research associate Jobs in Shawnee Ks

Clinical Research Associate, Full Service
IQVIA —Overland Park, KS
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
CRA 1, IQVIA Biotech
IQVIA —Overland Park, KS
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
Clinical Research Coordinator I
U.S. Dermatology Partners —Leawood, KS
- $55,000 - $65,000 a year
- Full-time
- Vital signs
- Microsoft Outlook
- Computer literacy
- Paid holidays
- Health insurance
Quick Apply
11d
Quality Control Associate
DR VINCE CLINICAL RESEARCH PA —Overland Park, KS
- Full-time
- High school diploma or GED
- Bachelor's degree
- Entry level
Quick Apply
9d
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 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 Assistant II
Children's Mercy KC —Kansas City, MO
- From $24.14 an hour
- Full-time
- Pass drug screening
- Mid-level
- 3 years
6d
Clinical Research Coordinator, On-Site
IQVIA —Kansas City, MO
- $37,800 - $94,500 a year
- Full-time
- Patient monitoring
- Mid-level
- Office
12d
Clinical Research Coordinator - Women's Health Department
University Health KC —Kansas City, MO
- Full-time
- Hospital
- Computer literacy
- HIPAA
Contract Clinical Research Coordinator
IQVIA —Kansas City, MO
- $62,800 - $157,100 a year
- Full-time
- Mid-level
- 3 years
- Medical terminology
Clinical Research Assistant - Internal Medicine (Pulmonary, Critical Care, and Sleep Medicine)
The University of Kansas Medical Center —Kansas City, MO
- $22.88 - $33.17 an hour
- Full-time
- Nursing
- Computer literacy
- Internal Medicine
- Paid jury duty
- Paid holidays
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
Patient Recruitment Coordinator
Johnson County Clintrials LLC —Lenexa, KS
- $20 - $22 an hour
- Full-time
- Hybrid work
- HIPAA
- Mid-level
- High school diploma or GED
Quick Apply
6d
Research Assistant
Johnson County Clintrials LLC —Kansas City, MO
- $25 an hour
- Full-time
- Microsoft Excel
- Vital signs
- Microsoft Outlook
Quick Apply
11d
Phlebotomist - Clinical Research Technician II
Altasciences —Overland Park, KS
- Full-time
- Customer service
- English
- Mid-level
- Paid holidays
- Health 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
Site Enrollment and Engagement Lead - National - PAH/IPF
IQVIA —Overland Park, KS
- $62,300 - $195,100 a year
- Full-time
- Nursing
- RN License
- Sales
- Work from home
Senior Clinical Research Coordinator - Pediatrics
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
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
Clinical Research Supervisor - Internal Medicine (All of Us Research Program)
The University of Kansas Medical Center —Kansas City, MO
- $80,600 - $120,900 a year
- Weekends as needed
- Inventory management
- Internal Medicine
- Mid-level
- Paid jury duty
- Paid holidays

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Clinical Research Associate, Full Service

IQVIA -
Overland Park, KS

Apply Now

Job Details

Full-time
$47,400 - $169,300 a year

Qualifications

Computer literacy
Employee relationship building

Full Job Description

Overland Park, United States of America | Full time | Field-based | R1497311

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

Bachelor's Degree Degree in scientific discipline or health care preferred. Req
Equivalent combination of education, training and experience may be accepted in lieu of degree.
Some organizations require completion of CRA training program or prior monitoring experience.
Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
Good therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Written and verbal communication skills including good command of English language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

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, when annualized, is $47,400.00 - $169,300.00. 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

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

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 research associate jobs in shawnee ks

Clinical Research Associate, Full Service

CRA 1, IQVIA Biotech

Clinical Research Coordinator I

Quality Control Associate

Senior Clinical Research Associate, Sponsor Dedicated

Clinical Research Assistant - Cancer Center

Clinical Research Assistant II

Clinical Research Coordinator, On-Site

Clinical Research Coordinator - Women's Health Department

Contract Clinical Research Coordinator

Clinical Research Assistant - Internal Medicine (Pulmonary, Critical Care, and Sleep Medicine)

Senior Clinical Research Associate, Sponsor Aligned, Oncology

Patient Recruitment Coordinator

Research Assistant

Phlebotomist - Clinical Research Technician II

Clinical Research Coordinator - Internal Medicine (Nephrology)

Site Enrollment and Engagement Lead - National - PAH/IPF

Senior Clinical Research Coordinator - Pediatrics

Senior Clinical Research Coordinator - Cancer Center

Clinical Research Supervisor - Internal Medicine (All of Us Research Program)

I want to receive the latest job alert for clinical research associate in shawnee ks

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