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Act as a subject matter expert by answering research questions and providing feedback on ITSM/ESM platforms. Participate in surveys, interviews, and scenario reviews to inform the development of AI models and IT operations processes.
Provide expert insights and feedback on ITSM/ESM platforms through research questions, scenario reviews, and interviews. Contribute subject matter expertise to help research teams understand how IT functions evaluate service management tools.
Provide expert insights and feedback on ITSM/ESM platforms through research questions, scenario reviews, and interviews. Contribute subject matter expertise to help research teams understand how IT functions evaluate service management tools.
Provide expert insights and feedback on ITSM/ESM platforms through research questions, scenario reviews, and interviews. Contribute subject matter expertise to help research teams understand how IT functions evaluate service management tools.
Provide expert insights and feedback on ITSM/ESM platforms through research questions, scenario reviews, and interviews. Contribute subject matter expertise to help research teams understand how IT functions evaluate service management tools.
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Provide expert insights and feedback on ITSM/ESM platforms through research questions, scenario reviews, and interviews. Contribute subject matter expertise to help research teams understand how IT functions evaluate service management platforms.
Act as a subject matter expert by answering research questions and providing feedback on ITSM/ESM platforms. Participate in surveys, interviews, and scenario reviews to inform the development of AI models and service management practices.
Provide expert insights and feedback on HR and People Operations workflows, specifically regarding ITSM/ESM platforms. Participate in research tasks, surveys, and interviews to inform the development of AI models.
Provide expert insights and feedback on HR and People Operations workflows through research questions, surveys, and interviews. Assess real-world scenarios related to internal ticketing, onboarding, and service management platforms.
Provide expert insights and feedback on HR and People Operations workflows through research questions, surveys, and interviews. Assess real-world scenarios related to internal ticketing, onboarding, and service management platforms.
Design and implement evaluation pipelines and observability tools to analyze and improve AI coding agent behavior for Kotlin. Research post-training techniques and build open-source benchmarks to establish industry standards for Kotlin AI performance.
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
The specialist will design and implement enterprise knowledge management systems, including metadata frameworks and taxonomies to improve organizational discovery. They will also evaluate KM platforms and serve as a Data Steward to ensure compliance with data governance standards.
The Senior CRA is responsible for the preparation, initiation, monitoring, and closure of clinical study sites in compliance with international guidelines and local regulations. Key duties include performing site visits, verifying source data, and ensuring the quality and integrity of collected study data.
The Senior CRA is responsible for monitoring clinical study sites remotely and on-site to ensure trials are conducted according to protocols, SOPs, and ICH GCP guidelines. Key duties include conducting site visits, verifying source data, and managing action item resolution to ensure regulatory compliance.
The CRA II is responsible for monitoring clinical study sites remotely and onsite to ensure trials are conducted according to protocols, SOPs, and ICH GCP guidelines. Key duties include conducting site visits, verifying source data, and managing site staff training and compliance.
The role involves coordinating the setup and monitoring of clinical trials, ensuring accurate study status reports and documentation. It also requires maintaining collaborative relationships with investigators and ensuring strict compliance with regulatory requirements and patient safety.
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The role involves coordinating and monitoring clinical trial activities, ensuring accurate study status reports and documentation. It also requires maintaining strong relationships with investigators and ensuring patient safety through regulatory compliance.
Support the medical and scientific aspects of global clinical studies for rare diseases, including acting as a medical monitor and contributing to the Common Technical Document. Collaborate with internal and external stakeholders to ensure the design, conduct, and interpretation of clinical trials align with business strategy and patient needs.
Manage a team of EMR Analysts to interpret clinical protocols and translate them into detailed schedules of events. Serve as a clinical expert to validate protocol interpretation and manage the amendment intake process to ensure trial accuracy and compliance.
Manage a team of EMR Analysts to interpret clinical protocols and translate them into detailed schedules of events. Serve as a clinical expert to validate protocol interpretations and manage the amendment intake process to ensure trial accuracy and compliance.
Manage research activities at clinical sites, including site identification, start-up activities, and regulatory document collection. Conduct study initiation visits and ensure compliance with informed consent and safety reporting throughout the study lifecycle.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage and deliver full clinical site monitoring services, including the design and oversight of project monitoring, site recruitment, and regulatory filings. Act as a Lead CRA to mentor peers and serve as the primary liaison between the project team and sponsors.
This senior analyst is responsible for the implementation, support, and architecture of Epic Research applications within the Mount Sinai landscape. The role involves leading project tasks, defining system requirements with business partners, and monitoring project lifecycles from initiation to completion.
Design and implement robust data pipeline tooling for synthesis, analysis, and management of real and synthetic data. Collaborate with ML modeling teams to establish standardized processes for data validation and benchmark coverage gaps.
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Challenge and improve bot detection mechanisms through red teaming and the creation of automation tools. Enhance client-side detection by implementing browser fingerprinting, JavaScript obfuscation, and SDK signal collection.
The role involves coordinating and monitoring clinical trials to ensure high-quality outcomes and patient safety. Key tasks include managing study documentation, running sponsor queries, and maintaining relationships with clinical investigators and site staff.
Responsible for site management, monitoring, and close-out of clinical trial investigator sites to ensure patient safety and quality execution. This includes managing operational activities from site activation to database lock and coordinating with study teams and vendors.
Coordinate day-to-day remote clinical trial operations, including facilitating remote patient visits and managing data entry in EDC and CTMS systems. Serve as a virtual liaison between sponsors, CROs, and internal site teams while ensuring regulatory compliance.
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