Manages the team responsible for monitoring clinical research trials across multiple study sites. 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. Reviews and verifies data collected is accurate and complete. Assists with design, development, and monitoring of clinical evaluation projects. Requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a director. 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. 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.
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.
Leads and manages the team responsible for monitoring clinical research trials across multiple study sites. 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. Reviews and verifies data collected is accurate and complete. Contributes to the design and development of clinical evaluation projects. Requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a director. Typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. Typically requires 3+ years of managerial experience. Capable of resolving escalated issues arising from operations and requiring coordination with other departments.
Supervises the team responsible for monitoring clinical research trials across multiple study sites. 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. 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. 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. Typically requires 3-5 years experience in the related area as an individual contributor. Thorough knowledge of functional area and department processes.
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.