There is currently no job description for Onsite Manager, be the first to
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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 Monitor III 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 III may assist with design, development, and monitoring of clinical evaluation projects. Verifies data collected is accurate and complete. In addition, Clinical Research Onsite Monitor III requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Being a Clinical Research Onsite Monitor III work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. Working as a Clinical Research Onsite Monitor III typically requires 4-7 years of related experience.
The Clinical Research Onsite Monitor V 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 V may assist with design, development, and monitoring of clinical evaluation projects. Verifies data collected is accurate and complete. In addition, Clinical Research Onsite Monitor V requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Being a Clinical Research Onsite Monitor V works autonomously. Goals are generally communicated in "solution" or project goal terms. May provide a leadership role for the work group through knowledge in the area of specialization. Works on advanced, complex technical projects or business issues requiring state of the art technical or industry knowledge. Working as a Clinical Research Onsite Monitor V typically requires 10+ years of related experience.
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