Top 85 Clinical research coordinator Jobs in Lenexa Ks

Clinical Research Associate, Full Service
5PY IQVIA RDS Inc. —Overland Park, KS
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
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
8d
Clinical Research Associate, Full Service
IQVIA —Overland Park, KS
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Clinical Care Coordinator
Aria Care Partners —Overland Park, KS
- Full-time
- Office
- Quality control
- Experience equivalent to degree accepted
- Health savings account
- Paid holidays
Quick Apply
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
14d
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
9d
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
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 Assistant II
Children's Mercy KC —Kansas City, MO
- From $24.14 an hour
- Full-time
- Pass drug screening
- Mid-level
- 3 years
3d
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
14d
Inpatient Clinical Research Nurse Coordinator
The University of Kansas Health System —Kansas City, KS
- Part-time
- Nursing
- RN License
- Hospital
9d
Clinical Research Coordinator II- Nephrology
Johnson County Clintrials LLC —Kansas City, MO
- $27 - $32 an hour
- Full-time
- Vital signs
- Microsoft Outlook
- Bachelor of Science
Quick Apply
1d
Phlebotomist - Clinical Research Technician II
Altasciences —Overland Park, KS
- Full-time
- Mid-level
- High school diploma or GED
- Clinic
- Paid holidays
- Health insurance
7d
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
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
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
Clinical Research Nurse Coordinator- Cardiology
The University of Kansas Medical Center —Kansas City, MO
- $70,200 - $105,300 a year
- Full-time
- Nursing
- 6 years
- RN License
- Paid jury duty
- Paid holidays
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
3d

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Clinical Research Associate, Full Service

5PY IQVIA RDS Inc. -
Overland Park, KS

Apply Now

Job Details

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

Qualifications

Computer literacy
Employee relationship building

Full Job Description

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.

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Refine Your Search

clinical research coordinator jobs in lenexa ks

Clinical Research Associate, Full Service

Clinical Research Coordinator I

Clinical Research Associate, Full Service

Clinical Care Coordinator

Clinical Research Coordinator - Women's Health Department

Contract Clinical Research Coordinator

Senior Clinical Research Associate, Sponsor Dedicated

Clinical Research Coordinator, On-Site

Senior Clinical Research Coordinator - Pediatrics

Clinical Research Coordinator - Internal Medicine (Nephrology)

Clinical Research Assistant II

Clinical Research Assistant - Cancer Center

Inpatient Clinical Research Nurse Coordinator

Clinical Research Coordinator II- Nephrology

Phlebotomist - Clinical Research Technician II

Senior Clinical Research Coordinator - Cancer Center

Senior Clinical Research Associate, Sponsor Aligned, Oncology

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

Clinical Research Nurse Coordinator- Cardiology

Senior Regulatory Coordinator - Comprehensive Integrated Research Operations (CIRO)

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