There is currently no job description for Onsite Manager, be the first to
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the job responsibilities for Onsite Manager.
The Clinical Research Onsite 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 Research Onsite Monitoring Manager assists with design, development, and monitoring of clinical evaluation projects. Reviews and verifies data collected is accurate and complete. In addition, Clinical Research Onsite Monitoring Manager requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a director. The Clinical Research Onsite 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 Research Onsite 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.
The Clinical Research Onsite Monitoring Senior 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. Leads and manages the team responsible for monitoring clinical research trials across multiple study sites. Being a Clinical Research Onsite Monitoring Senior Manager contributes to the design and development of clinical evaluation projects. Reviews and verifies data collected is accurate and complete. In addition, Clinical Research Onsite Monitoring Senior Manager requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a director. The Clinical Research Onsite 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. Working as a Clinical Research Onsite Monitoring Senior Manager typically requires 3+ years of managerial experience. Capable of resolving escalated issues arising from operations and requiring coordination with other departments.
There is currently no job description for Business Development Center Manager, be the first to
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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.