Central Monitor II Salary in Omaha, NE

Central Monitor - Average Salary $44,826

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Clinical Research Monitor II - Average Salary $73,330

Responsible for monitoring clinical research trials across multiple study sites. 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. Verifies data collected is accurate and complete. May assist with design, development, and monitoring of clinical evaluation projects. Requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. Typically requires 2-4 years of related experience.

Clinical Data Monitor II - Average Salary $73,400

The Clinical Data 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 Data Monitor II may assist with design, development, and monitoring of clinical evaluation projects. Verifies data collected is accurate and complete. In addition, Clinical Data Monitor II requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Being a Clinical Data 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 Data Monitor II typically requires 2-4 years of related experience.

Pipeline Control Monitor Technician II - Average Salary $82,155

Operates and monitors pipeline systems. Consistently evaluates and responds to flow rate and system pressure metrics to maintain quality, reduce contamination, and reduce risk of emergency. Responds to alarms and emergencies by executing appropriate procedures and plans, including directing appropriate personnel such as scheduling, operations, and maintenance specialists. Troubleshoots alarms and issues, including product quality and measurement issues, and suggests improvements. Interfaces with schedules and schedulers to ensure the proper delivery of products, and to provide helpful feedback. Requires a high school diploma or equivalent. Typically reports to a supervisor or manager. Works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. Typically requires 1-3 years of related experience.

Clinical Research Onsite Monitor II - Average Salary $73,340

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.