RN UnityPoint Work Onsite Salary in Mississippi
How Much Does a RN UnityPoint Work Onsite make?
RN UnityPoint Work Onsite made a median salary around $77,287 in March, 2025.
The best-paid 25 percent made $85,966 probably that year, while the lowest-paid 25 percent made around $70,083.
Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills, the number of years you have spent in your profession.
With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target.
Check out
RN UnityPoint Work Onsite
jobs in
Mississippi
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Best-Paying Cities for RN UnityPoint Work Onsite
The metropolitan areas that pay the highest salary in the RN UnityPoint Work Onsite profession are Centreville
, Chatawa
, Crosby
, Fernwood
, Gloster
.
| Centreville, MS | $81,619 |
| Chatawa, MS | $81,619 |
| Crosby, MS | $81,619 |
| Fernwood, MS | $81,619 |
| Gloster, MS | $81,619 |
Best-Paying States for RN UnityPoint Work Onsite
The states and districts that pay RN UnityPoint Work Onsite the highest salary are District of Columbia (around $96,435)
, California (around $95,569)
, New Jersey (around $94,962)
, Alaska (around $94,356)
, and Massachusetts (around $94,269)
.
| District of Columbia | $96,435 |
| California | $95,569 |
| New Jersey | $94,962 |
| Alaska | $94,356 |
| Massachusetts | $94,269 |
What is the Career Path of RN UnityPoint Work Onsite?
A career path is a sequence of jobs that leads to your short- and long-term career goals. Some follow a linear career path within one field, while others change fields periodically to achieve career or personal goals.
For RN UnityPoint Work Onsite, the first career path typically progresses to Head Nurse - CCU.
The second career path typically progresses to Maternity Services Director.
The third career path typically progresses to Head Nurse - Emergency Room.
Additionally, the fourth career path typically starts with a Head Nurse - Intensive Care Unit position , and then progresses to Head of Intensive Care Unit.
Besides, RN UnityPoint Work Onsite can also turn to other related jobs, including
RN WEEKENDS WORK LIFE BALANCE
,
Clinical Research Onsite Monitor IV
,
Clinical Research Onsite Monitor II
and
Clinical Research Onsite Monitor III
.
Frequently Asked Questions for RN UnityPoint Work Onsite
Q:
What is the salary range of RN UnityPoint Work Onsite in Mississippi?
A:
In 2025
, the lowest-paid RN UnityPoint Work Onsite in Mississippi earned an average annual salary of $70,083
, while the highest-paid made $85,966.
Q:
What is the salary for a RN UnityPoint Work Onsite in California?
A:
RN UnityPoint Work Onsite employed in California earned an average salary of $95,569 in 2025.
Average RN UnityPoint Work Onsite Pay vs. Other Jobs
RN UnityPoint Work Onsite earned an average salary of $77,287 in 2025.
Other jobs related to RN UnityPoint Work Onsite earned the following average salary in March, 2025.
RN WEEKENDS WORK LIFE BALANCE
made $64,315
,
Clinical Research Onsite Monitor IV
made $137,720
,
Clinical Research Onsite Monitor II
and
Clinical Research Onsite Monitor III
made $91,680
and $115,070 respectively
.
Relevant Jobs of RN UnityPoint Work Onsite
There is currently no job description for RN WEEKENDS WORK LIFE BALANCE, be the first to
submit
the job responsibilities for RN WEEKENDS WORK LIFE BALANCE.
The Clinical Research Onsite Monitor IV ensures all clinical research trials are conducted, recorded, and reported in adherence to established processes and procedures, FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and all other applicable regulatory requirements. Responsible for monitoring clinical research trials across multiple study sites. Being a Clinical Research Onsite Monitor IV may assist with design, development, and monitoring of clinical evaluation projects. Verifies data collected is accurate and complete. In addition, Clinical Research Onsite Monitor IV requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Being a Clinical Research Onsite Monitor IV work is highly independent. May assume a team lead role for the work group. A specialist on complex technical and business matters. Working as a Clinical Research Onsite Monitor IV typically requires 7+ years of related experience.
The Clinical Research Onsite Monitor II ensures all clinical research trials are conducted, recorded, and reported in adherence to established processes and procedures, FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and all other applicable regulatory requirements. Responsible for monitoring clinical research trials across multiple study sites. Being a Clinical Research Onsite Monitor II may assist with design, development, and monitoring of clinical evaluation projects. Verifies data collected is accurate and complete. In addition, Clinical Research Onsite Monitor II requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Being a Clinical Research Onsite Monitor II occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. Working as a Clinical Research Onsite Monitor II typically requires 2-4 years of related experience.
The Clinical Research Onsite Monitor III ensures all clinical research trials are conducted, recorded, and reported in adherence to established processes and procedures, FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and all other applicable regulatory requirements. Responsible for monitoring clinical research trials across multiple study sites. Being a Clinical Research Onsite Monitor III may assist with design, development, and monitoring of clinical evaluation projects. Verifies data collected is accurate and complete. In addition, Clinical Research Onsite Monitor III requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Being a Clinical Research Onsite Monitor III work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. Working as a Clinical Research Onsite Monitor III typically requires 4-7 years of related experience.
The Clinical Research Onsite Monitor I ensures all clinical research trials are conducted, recorded, and reported in adherence to established processes and procedures, FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and all other applicable regulatory requirements. Responsible for monitoring clinical research trials across multiple study sites. Being a Clinical Research Onsite Monitor I may assist with design, development, and monitoring of clinical evaluation projects. Verifies data collected is accurate and complete. In addition, Clinical Research Onsite Monitor I requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Being a Clinical Research Onsite Monitor I work is closely managed. Works on projects/matters of limited complexity in a support role. Working as a Clinical Research Onsite Monitor I typically requires 0-2 years of related experience.