Build and maintain Apache Airflow DAGs and SageMaker training jobs for NLP model orchestration. Implement MLflow tracking and infrastructure-as-code using Terraform for AWS services.
Remote Jobs & Work From Home Opportunities (1,769)
Search = Research
Support the management of clinical trial sites by conducting monitoring visits and ensuring compliance with SOPs and ICH-GCP guidelines. Perform source data verification and maintain essential trial documentation to ensure data quality and inspection readiness.
Coordinate care for patients in clinical research studies and facilitate communication between participants and healthcare providers. Monitor patient progress and collect accurate data while ensuring strict compliance with regulatory standards.
Lead and mentor a polyglot engineering team while managing recruiting, performance, and career development. Bridge the gap between R&D prototypes and scalable production systems while translating technical progress for business stakeholders.
Lead and mentor a polyglot engineering team while managing recruiting, performance, and career development. Bridge the gap between R&D prototypes and scalable production systems while interfacing with non-engineering partners.
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Coordinate site and operational activities for global clinical trials from start-up to close. Perform Imaging Quality Control (IQC) activities and maintain study databases to ensure data accuracy and compliance.
Lead and mentor a high-performing offensive security research team focused on vulnerability discovery and exploit development. Oversee technical strategy, manage team budgets, and coordinate cross-team initiatives to align with organizational priorities.
Senior Research Engineer - Solution Engineering Team
Tenable, Inc.
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Full Time
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7 Weeks Ago
Tenable, Inc.
The role acts as a bridge between Research and Product teams to transform novel security concepts into MVPs and production-ready systems. Responsibilities include designing scalable architectures and collaborating cross-functionally to drive technology transfer.
The CRA II will independently monitor Phase II-IV clinical trials for a global pharmaceutical partner, ensuring compliance with ICH-GCP and sponsor SOPs. Key tasks include conducting site visits, managing study documentation, and maintaining strong relationships with investigators across various therapeutic areas.
Manage and sell Research Intelligence solutions to academic and government institutions across specific US states. Focus on achieving revenue targets through consultative selling, strategic account planning, and maintaining relationships with key decision-makers.
Administrative Research Assistant
Research Foundation of The City University of New York
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Full Time
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7 Weeks Ago
Research Foundation of The City University of New York
The role involves coordinating core research team operations, including participant coordination, data collection, and digital file management. Additionally, the assistant provides financial and grant support by tracking expenses and ensuring compliance with reporting processes.
Conduct comprehensive market research to provide clients and recruitment teams with data on talent supply, demand, and salary benchmarking. Produce high-quality deliverables and reports that summarize industry trends and identify effective sourcing channels.
The CRA II is responsible for managing clinical site relationships and ensuring protocol compliance through remote and on-site monitoring activities. They conduct various site visits, manage regulatory documentation, and collaborate cross-functionally to ensure data accuracy and subject safety.
The Senior CRA is responsible for managing clinical site relationships and ensuring protocol compliance through monitoring activities in accordance with ICH-GCP and regulatory standards. This includes conducting site visits, managing regulatory documentation, and collaborating cross-functionally to ensure data accuracy and subject safety.
Clinical Research Associate (CRA) - Client-dedicated
Thermo Fisher Scientific
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Full Time
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7 Weeks Ago
Thermo Fisher Scientific
Perform and coordinate all aspects of the clinical monitoring process independently. Provide end-to-end support for clinical trials from study start-up through to close-out.
The Senior Clinical Research Associate will contribute to the advancement of clinical research by supporting various medical discovery projects. They will work collaboratively within a performance-driven environment to embed innovation into company processes.
Research Administrator, Pre-Award III - School of Medicine - Pediatrics
Emory University
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Full Time
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7 Weeks Ago
Emory University
The Research Administrator manages pre-award activities for a portfolio of grants and contracts, ensuring adherence to agency and university guidelines. They also provide guidance to team members and coordinate workload distribution within the Research Administration Services unit.
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Clinical Research Site Manager (Neurology)
Johns Hopkins University
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Full Time
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7 Weeks Ago
Johns Hopkins University
The Clinical Research Site Manager oversees the site-level execution of large, multicenter clinical trials by leading site startup, driving enrollment performance, and managing investigator relationships. They are responsible for ensuring protocol fidelity, regulatory compliance, and consistent performance across a national network of collaborating clinical sites.
Sr. Clinical Research Manager (Neurology)
Johns Hopkins University
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Full Time
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7 Weeks Ago
Johns Hopkins University
The Sr. Clinical Research Manager directs clinical research operations, manages the clinical trials portfolio, and collaborates with investigators to set research direction. They are responsible for staff supervision, regulatory compliance, budget management, and ensuring the efficient conduct of research protocols.
Senior Editor, Research & Intelligence
Black & White Zebra
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Full Time
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7 Weeks Ago
Black & White Zebra
The Senior Editor will gather audience insights through research and interviews to shape content, products, and growth strategies. They will lead the development of insight-driven content and establish repeatable systems to improve subscriber conversion and audience engagement.
Conduct cutting-edge machine learning research to build and train large language models. Contribute to research initiatives that have practical applications in product development and disseminate findings through publications and code.
You will develop and execute content and research strategies while managing the creation and distribution of complex industry-related materials. Additionally, you will analyze marketing performance using KPIs and collaborate with internal stakeholders to optimize content impact.
The Senior Clinical Research Scientist will support the design, development, and execution of clinical studies, ensuring overall study quality in alignment with GCP and regulatory expectations. This role involves comprehensive data review, risk identification, and collaboration with cross-functional teams.
Design and operate high-throughput, fault-tolerant systems for large-scale web data acquisition and model development. Collaborate with research teams to build data pipelines for cleaning, filtering, and normalizing billions of web pages.
The Clinical Research Associate conducts site monitoring visits to ensure clinical trial protocol compliance, data integrity, and adherence to regulatory standards. They also provide leadership and guidance to study sites while collaborating with cross-functional teams to manage trial execution and safety reporting.
The Medical Science Liaison will engage academic KOLs and investigators to facilitate collaborative external research and provide medical support for strategic account management. They will also serve as a research liaison between internal data scientists and external investigators while contributing to the management of the external research portfolio.
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The ML Research Engineer will bridge research and engineering teams to take machine learning models from experimentation to production. They will also establish engineering standards and mentor team members on best practices for production environments.
The Clinical Research Associate II is responsible for monitoring clinical study sites to ensure trials are conducted in accordance with protocols, SOPs, and regulatory requirements. They perform site visits, conduct source data verification, and facilitate the resolution of action items while maintaining compliance with ICH GCP standards.
You will define the research direction for A1's core intelligence, focusing on reasoning, memory, planning, and orchestration. You will also establish evaluation frameworks to ensure real-world usefulness, safety, and robustness of the AI system.
The Site Director is responsible for the end-to-end management of clinical sites, including site identification, study start-up, monitoring, and close-out activities. They ensure compliance with protocols, ICH-GCP guidelines, and regulatory requirements while overseeing patient safety and data integrity.
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