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The SCRA is responsible for managing and overseeing clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines. They also provide mentoring to junior CRAs and collaborate with Clinical Study Teams to optimize site effectiveness and efficiency.
The Research Computing Assistant will assist staff in developing teaching materials, supporting workshops, and maintaining the RC website. Additional tasks include scientific software installations, consulting support, and administrative logistics for outreach events.
Lead the end-to-end quantitative research process to deliver actionable insights and strategic recommendations for brand growth and innovation. Manage project teams, oversee survey design and data analysis, and cultivate client relationships to drive new business growth.
The role involves coordinating clinical monitoring and site management, including source data verification and ensuring protocol and regulatory compliance. It requires conducting on-site and remote visits while collaborating with cross-functional teams to maintain audit readiness.
Collect and verify critical on-site property and tenant data to maintain the accuracy of the company's real estate database. Document building characteristics, occupancy, and available space to provide foundational intelligence for CoStar Group products.
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Manage research activities at clinical sites, including site identification, start-up, and close-down. Ensure compliance with regulatory requirements, informed consent, and safety reporting through remote and on-site monitoring.
Lead the Docugami Europe AI research lab by managing a team of researchers and PhD interns to advance cutting-edge AI technology. Collaborate with academic institutions and internal engineering teams to develop a long-term science roadmap and publish research findings.
The role focuses on researching and identifying creators and authors across platforms like TikTok, Instagram, YouTube, and LinkedIn. It involves analyzing digital trends and preparing communication materials and presentations for new partnerships.
Oversees clinical monitoring activities and manages the CRA team to ensure compliance with ICH-GCP and company SOPs. Leads resource allocation, performance management, and strategic initiatives to optimize clinical operations and trial delivery.
Apprentices will lead the end-to-end UX design and research process for a startup idea of their choice. This includes conducting discovery research, building digital products, and delivering a business pitch based on qualitative and quantitative data.
Apprentices will lead the end-to-end UX design and research process for a startup idea of their choice. This includes conducting discovery research, creating design systems, and delivering a business pitch based on qualitative and quantitative data.
Apprentices will lead the end-to-end UX design and research process for a startup idea of their choice. This includes conducting discovery research, creating visual deliverables, and developing a business model for their product.
Apprentices will lead the end-to-end UX design and research process for a startup idea of their choice. This includes conducting discovery research, creating visual deliverables, and developing a business model for their product.
Participate in various research studies to contribute to meaningful outcomes. Perform data entry tasks and follow specific study directions in a remote environment.
Participate in various research studies to contribute to meaningful outcomes. Perform data entry tasks and follow specific study instructions from a remote environment.
The Senior CRA is responsible for ensuring data integrity, quality, and compliance with ICH GCP and local requirements at the site level. This includes conducting virtual and on-site monitoring, managing protocol deviations, and collaborating with Site Managers to ensure inspection readiness.
The CRA II acts as the primary liaison between the project team, sponsor, and clinical sites to ensure high-quality study conduct. Responsibilities include performing site selection, initiation, routine monitoring, and close-out visits while managing data integrity and compliance.
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Research and develop offensive agentic capabilities and LLM-powered tooling to automate vulnerability discovery. Own the end-to-end process from research spikes to production deployment of customer-facing features.
Lead the Research Solutions team by managing complex quantitative research projects and maintaining high-level client relationships. Drive account growth and ensure the delivery of strategic insights to inform critical business decisions.
Provide elite-level consultancy on model behavior and domain-specific logic to help design and evaluate advanced generative AI systems. Collaborate with research teams to co-author technical reports and represent the collective as a subject matter expert during executive engagements.
Participate in various research studies to contribute to meaningful outcomes. Perform data entry tasks and follow specific study directions from a remote environment.
Participate in various research studies to contribute to meaningful outcomes. Perform data entry tasks and follow instructions to earn income from home.
The Sr. CRA is responsible for managing investigative sites and performing monitoring activities throughout the clinical trial lifecycle to ensure data integrity and subject safety. Key duties include conducting site visits, managing essential documents, and ensuring compliance with protocols and regulatory standards.
Manage all aspects of clinical site management from selection to close-out for Phase I-III studies. Provide mentoring and training for new employees and serve as a subject matter expert in customer-specific working groups.
Conduct AI-driven market research on education and employment trends to identify growth opportunities. Support marketing efforts through data administration, content drafting, and creative design for digital campaigns.
The Senior Clinical Research Associate is responsible for site management, monitoring, and close-out of clinical trial investigator sites to ensure patient safety and quality study execution. They manage investigator site relationships and resolve protocol-related issues while ensuring compliance with applicable laws and standards.
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The Site Director manages overall clinical site operations, including identification, start-up, monitoring, and close-out of Phase I-IV studies. They ensure patient safety, data accuracy, and compliance with ICH-GCP guidelines and regulatory requirements.
Participate in various research studies to contribute to meaningful outcomes. Perform data entry tasks and follow specific study instructions in a remote environment.
The Research Manager provides analytic leadership and project coordination for an interdisciplinary research program focused on epidemiology and cancer outcomes. Key duties include managing data governance, contributing to grant applications, and overseeing the development of manuscripts and reports.
Lead and develop computational research projects focused on discovering small molecule modulators for pediatric diseases. Responsibilities include developing new computational methods, analyzing data, and mentoring other researchers.
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