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The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
Support the research and analysis of social and climate impacts for existing and potential investments. Contribute to impact assessments for climate-related deals and conduct in-depth reviews of academic research.
The CRA II will monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Responsibilities include coordinating site setup, conducting initiation visits, and managing the overall progress of clinical trials.
The CRA II will monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Responsibilities include coordinating site setup, conducting initiation visits, and managing regulatory submissions.
The Research Analyst is responsible for maintaining data quality and coverage for the HCP Universe product. This includes validating conference and clinical trial data and synthesizing secondary research into structured information.
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Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. Conduct site visits to assess performance, resolve issues, and collaborate with cross-functional teams for accurate data reporting.
Serve as a pathology subject-matter expert to support biomarker and diagnostic programs, including companion diagnostics and molecular pathology. Translate clinical and histopathologic knowledge into actionable guidance for AI/ML model design, validation, and interpretation.
Participate in research studies to contribute to meaningful outcomes. Perform data entry tasks and follow instructions to earn income from home.
Participate in various research studies to contribute to meaningful outcomes. Perform data entry tasks and research activities from a remote home environment.
Lead a team of 5-7 researchers to shape AI-powered human capital management experiences and influence product direction. Partner with cross-functional leaders to align research with business value and evolve research operations for scalability.
Lead a team of 5-7 researchers to shape AI-powered human capital management experiences and influence product direction. Partner with cross-functional leaders to align research with business value and evolve research operations for scalability.
The CRA is responsible for overseeing the quality, integrity, and compliance of clinical trial sites through qualification, initiation, and routine monitoring visits. They serve as the primary point of contact for sites, ensuring adherence to protocols, SOPs, and ICH GCP guidelines.
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data query resolution.
Serve as the executive relationship owner for a portfolio of oncology research sites to drive engagement and clinical trial enrollment growth. Align enterprise strategies with site goals while navigating complex matrixed environments to remove barriers and deliver value.
The CRA II will monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Responsibilities include coordinating study setup activities, identifying investigators, and preparing regulatory submissions.
The CRA II will monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Responsibilities include coordinating site setup, conducting initiation visits, and managing regulatory submissions.
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data query resolution.
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Design and execute research projects to support the training, evaluation, and use of LLM-based guardrails. Develop a robust alignment strategy combining state-of-the-art evaluation and optimization techniques for AI agents.
The role focuses on conducting product research and gathering market insights specifically for the US market. It supports the company's goal of reimagining the telco industry through its SaaS platform and digital brands.
Monitor and manage clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Coordinate study set-up activities and provide mentorship to junior staff while interacting directly with clients.
Monitor and manage clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Coordinate study set-up activities, mentor junior staff, and interact with clients regarding proposals and payments.
Ensure regulatory requirements for clinical trials are met by managing study binders and submitting protocol amendments to the IRB. Coordinate with clinical teams, sponsors, and federal agencies to document adverse events and maintain trial correspondence.
Participate in research studies to contribute to meaningful outcomes. Perform data entry tasks and follow specific study directions in a remote environment.
Participate in research studies to contribute to meaningful outcomes. Perform data entry tasks and utilize a computer or smartphone to complete assigned studies.
The role involves coordinating the setup and monitoring of clinical trials, ensuring accurate study status reports and documentation. It also requires maintaining strong relationships with investigators and ensuring patient safety through regulatory compliance.
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. They also perform data review and collaborate with investigators to maintain high-quality clinical data.
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The Research Consultant manages end-to-end client relationships and the full project life cycle for survey-based research. They synthesize complex data into actionable insights and strategic recommendations to influence business decisions for leading brands.
Bridge the gap between threat research and production by turning research artifacts into scalable detection rules, feeds, and APIs. Build and maintain the STRIKE platform components, including OSINT ingestion and automation workflows for indicator enrichment.
Bridge the gap between threat research and production by turning research artifacts into scalable detection rules, feeds, and APIs. Build and maintain the STRIKE platform components, including OSINT ingestion and sandbox orchestration, while automating research workflows.
Bridge the gap between threat research and production by turning research artifacts into deployable detection rules, feeds, and APIs. Build and maintain the STRIKE platform components and automate research workflows using language models and data pipelines.
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