Also referred to as:
Clinical Data Monitoring Senior Manager, Clinical Research Onsite Monitoring Senior Manager
Requirements and Responsibilities
Clinical Research Monitoring Senior Manager 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. Being a Clinical Research Monitoring Senior Manager reviews and verifies data collected is accurate and complete. Contributes to the design and development of clinical evaluation projects. Additionally, Clinical Research Monitoring Senior Manager requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a director. The Clinical Research Monitoring Senior Manager 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. To be a Clinical Research Monitoring Senior Manager typically requires 3+ years of managerial experience. Capable of resolving escalated issues arising from operations and requiring coordination with other departments.
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