Data Safety and Monitoring Board Manager Salary in Winston Salem, NC

Clinical Data Monitoring Manager - Average Salary $147,000

The Clinical Data Monitoring Manager oversees and 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. Manages the team responsible for monitoring clinical research trials across multiple study sites. Being a Clinical Data Monitoring Manager assists with design, development, and monitoring of clinical evaluation projects. Reviews and verifies data collected is accurate and complete. In addition, Clinical Data Monitoring Manager requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a director. The Clinical Data Monitoring Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. Working as a Clinical Data Monitoring Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes.

Clinical Data Monitoring Supervisor - Average Salary $121,000

The Clinical Data Monitoring Supervisor monitors and 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. Supervises the team responsible for monitoring clinical research trials across multiple study sites. Being a Clinical Data Monitoring Supervisor may assist with design, development, and monitoring of clinical evaluation projects. Verifies data collected is accurate and complete. In addition, Clinical Data Monitoring Supervisor requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. The Clinical Data Monitoring Supervisor supervises a group of primarily para-professional level staffs. May also be a level above a supervisor within high volume administrative/production environments. Makes day-to-day decisions within or for a group/small department. Has some authority for personnel actions. Working as a Clinical Data Monitoring Supervisor typically requires 3-5 years experience in the related area as an individual contributor. Thorough knowledge of functional area and department processes.

Drug Safety Monitoring and Information Specialist I - Average Salary $70,200

The Drug Safety Monitoring and Information Specialist I reviews safety and medical information for the assigned products, including safety components of protocols and studies for assigned drugs. Responsible for collecting, monitoring, processing, and distributing adverse event reports and information queries for investigational and marketed products. Being a Drug Safety Monitoring and Information Specialist I typically reports to a supervisor or manager. May require a bachelor's degree in area of specialty. Working as a Drug Safety Monitoring and Information Specialist I typically requires 0-2 years of related experience. Works on projects/matters of limited complexity in a support role. Work is closely managed.

Drug Safety Monitoring and Information Specialist III - Average Salary $100,100

The Drug Safety Monitoring and Information Specialist III reviews safety and medical information for the assigned products, including safety components of protocols and studies for assigned drugs. Responsible for collecting, monitoring, processing, and distributing adverse event reports and information queries for investigational and marketed products. Being a Drug Safety Monitoring and Information Specialist III typically reports to a manager or head of a unit/department. May require a bachelor's degree. Working as a Drug Safety Monitoring and Information Specialist III typically requires 4 to 7 years of related experience. Contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature.

Drug Safety Monitoring and Information Specialist II - Average Salary $82,900

The Drug Safety Monitoring and Information Specialist II reviews safety and medical information for the assigned products, including safety components of protocols and studies for assigned drugs. Responsible for collecting, monitoring, processing, and distributing adverse event reports and information queries for investigational and marketed products. Being a Drug Safety Monitoring and Information Specialist II typically reports to a supervisor or manager. May require a bachelor's degree in area of specialty. Working as a Drug Safety Monitoring and Information Specialist II typically requires 2 to 4 years of related experience. Gains exposure to some of the complex tasks within the job function. Occasionally directed in several aspects of the work.