Top 270 Science Jobs in Overland Park 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
6d
Staff Chemist – Synthetic Chemistry and API Manufacturing
MRIGlobal —Kansas City, MO
- $82,300 - $95,000 a year
- Email
- Bachelor of Science
- 3 years
- Bachelor's degree
- Paid parental leave
- Paid holidays
Quick Apply
12d
ENVIRONMENTAL LABORATORY ANALYST
Little Blue Valley Sewer District —Independence, MO
- $29.42 - $38.69 an hour
- Full-time
- Clean driving record
- Mid-level
- Driver's License
- Health savings account
- Paid holidays
Quick Apply
6d
Principal Chemist - IPS-Synthesis & API Mfg
MRIGlobal —Kansas City, MO
- $117,000 - $125,000 a year
- Email
- Bachelor of Science
- Bachelor's degree
- Doctor of Philosophy
- Paid parental leave
- Paid holidays
Quick Apply
12d
QC Analyst
Momentum Staffing Group LLC —North Kansas City, MO
- $50,000 a year
- Bachelor of Science
- Bachelor's degree
- Communication skills
Quick Apply
5d
CRA 1, IQVIA Biotech
IQVIA —Overland Park, KS
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
NVIRONMENTAL LABORATORY ANALYST
Little Blue Valley Sewer District —Independence, MO
- $29.42 - $38.69 an hour
- Online Application
- Clean driving record
- Mid-level
- Driver's License
- Health savings account
- Paid holidays
Quick Apply
2d
Data And Research Specialist
The University of Kansas Health System —Overland Park, KS
- Full-time
- Mid-level
- High school diploma or GED
- Computer skills
6d
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
Botanist
Stantec —Overland Park, KS
- Full-time
- Background check
- Clean driving record
- Word processing
Assistant Scientist - Energy Environmental
Olsson —Kansas City, MO
- Full-time
- Construction site
- Driver's License
- Bachelor's degree
- Wellness program
- Health insurance
2d
Clinical Research Associate, Full Service
IQVIA —Overland Park, KS
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Assistant Study Operations
Altasciences —Overland Park, KS
- Full-time
- Vital signs
- Customer service
- High school diploma or GED
- Paid holidays
- Health insurance
Wildlife Biologist
Stantec —Overland Park, KS
- Full-time
- Background check
- Clean driving record
- Word processing
Microbiology Technician
Heartland Coca-Cola Bottling Company —Olathe, KS
- $27.30 - $29.60 an hour
- Full-time
- Background check
- Computer literacy
- Mid-level
- Health insurance
- Dental insurance
7d
Medical Lab Scientist I
Saint Luke's Health System —Overland Park, KS
- 12 hour shift
- Bachelor's degree
- 1 year
- Entry level
Assistant Environmental Scientist - Environmental & Regulatory Compliance (Kansas City)
Burns & McDonnell —Kansas City, MO
- Full-time
- Microsoft Excel
- Construction site
- Analysis skills
8d
Medical Laboratory Scientist II
AdventHealth Shawnee Mission —Shawnee Mission, KS
- $26.41 - $49.11 an hour
- Overtime
- Computer literacy
- English
- Mid-level
- Paid parental leave
- Disability insurance
Microbiologist I
Argenta —Shawnee, KS
- Full-time
- Background check
- Computer literacy
- Bachelor of Science
Quick Apply
23h
Staff Scientist III
Braun Intertec —Kansas City, KS
- $60,000 - $90,000 a year
- Online Application
- English
- Mid-level
- Office
14d

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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
6 days ago

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.

Apply Now

Refine Your Search

science jobs in overland park ks

Clinical Research Associate, Full Service

Staff Chemist – Synthetic Chemistry and API Manufacturing

ENVIRONMENTAL LABORATORY ANALYST

Principal Chemist - IPS-Synthesis & API Mfg

QC Analyst

CRA 1, IQVIA Biotech

NVIRONMENTAL LABORATORY ANALYST

Data And Research Specialist

Lab Coordinator, Chemistry

Botanist

Assistant Scientist - Energy Environmental

Clinical Research Associate, Full Service

Assistant Study Operations

Wildlife Biologist

Microbiology Technician

Medical Lab Scientist I

Assistant Environmental Scientist - Environmental & Regulatory Compliance (Kansas City)

Medical Laboratory Scientist II

Microbiologist I

Staff Scientist III

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