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Develop advanced algorithms for computational geometry, mesh generation, and discretization to improve simulation performance and accuracy. Collaborate with cross-functional teams to integrate these methods into engineering workflows for digital twins and autonomous systems.
Lead the cross-line strategy for AI/ML-enabled research capabilities to drive product and pricing innovation. Build and manage a team focused on developing reusable research tooling, modernizing workflows, and implementing automated model monitoring.
The Program Manager oversees clinical research compliance and quality assurance across business units while supporting Principal Investigators and coordinators with regulatory adherence. They are responsible for developing quality processes, participating in audits, and analyzing operational data to drive continuous improvement.
The Research Technologist coordinates laboratory operations, manages mouse colonies, and supports animal-based research experiments. They are responsible for ensuring regulatory compliance, developing experimental protocols, and training research personnel in specialized laboratory techniques.
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The specialist is responsible for identifying funding opportunities, writing competitive grant proposals, and managing the submission process across multiple university programs. Additionally, they conduct research and synthesize data on public health topics to inform program strategy and proposal narratives.
The Research Technologist coordinates laboratory operations, manages mouse colonies, and supports animal-based research experiments. They are responsible for ensuring regulatory compliance, developing experimental protocols, and training research personnel in laboratory techniques.
The Research Assistant will conduct literature reviews, manage data in EndNote, and prepare research reports on suicidism and oppression. They will also be responsible for summarizing articles and performing critical analysis to support the research project.
The Manager of Market Research & Insights serves as a business partner to operating groups, shaping research agendas and translating insights into strategic actions. They are also responsible for leading and managing a matrixed team of insights analysts to ensure high-quality research delivery and alignment with business goals.
You will own the strategy and business outcomes for GitLab's Secret Detection and Vulnerability Research functions. This involves managing the full lifecycle of detection content, from research and rule generation to validation and automated revocation.
The analyst will evaluate public market asset classes, develop recommended investment strategies, and present findings to the Enterprise Investment Policy Committee. They will also collaborate with advisors on manager interviews, client onboarding, and asset class education.
The analyst will evaluate public market asset classes, develop recommended investment strategies, and present findings to the Enterprise Investment Policy Committee. They will also collaborate with advisors on manager interviews, strategy placements, and client portfolio reviews.
The Clinical Director is responsible for planning and directing clinical research activities for oncology and hematology medicines across all phases of development. They provide medical oversight for clinical trials, analyze study findings, and collaborate with cross-functional teams to support regulatory submissions and drug development strategies.
The Research Interventionalist will lead community outreach and recruitment efforts for research studies targeting Chinese, Japanese, and Korean populations. They are responsible for translating study materials, managing community partnerships, and analyzing recruitment data to support research operations.
The Research Contract Negotiator is responsible for drafting, reviewing, and negotiating various research-related agreements to ensure compliance with institutional and federal regulations. They will collaborate with faculty, principal investigators, and sponsors to mitigate risks and support the institution's research mission.
The Senior Clinical Research Associate is responsible for independently setting up, monitoring, and closing out clinical study sites while ensuring adherence to ICH-GCP regulations. They will also manage regulatory submissions, handle sponsor queries, and contribute to study documentation and feasibility assessments.
The Associate Research Scientist will lead real-world evidence studies by preparing and performing data analyses and developing study protocols. They will serve as the analytics expert on cross-functional project teams and communicate results to internal and external stakeholders.
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The In-House Clinical Research Associate supports study execution by managing meeting logistics, tracking action items, and ensuring protocol compliance. They are responsible for maintaining Trial Master Files and collaborating with cross-functional teams to resolve site-level issues.
The Clinical Research Associate serves as the primary point of contact for investigative sites, ensuring protocol compliance, data integrity, and patient safety. They are responsible for site training, monitoring activities, and implementing risk-mitigation strategies to drive study performance.
The Associate Research Scientist will lead real-world evidence studies, including developing protocols, preparing analytic datasets, and performing data analyses. They will serve as the analytics expert on cross-functional project teams and communicate study results to internal and external stakeholders.
Monitor and interpret tax laws and regulatory developments across the U.S. and Canada to ensure organizational compliance. Partner with cross-functional teams to translate complex legislation into actionable insights for system and process updates.
The Associate Director will develop and execute real-world evidence strategies to support global patient access and the commercial success of Rezdiffra. This role involves designing and conducting observational, pragmatic, and implementation science studies while collaborating with cross-functional teams to ensure high-quality evidence generation.
The Research Data Coordinator will maintain and update research information, databases, and project files to ensure accuracy. They will also assist project teams by preparing reports and identifying inconsistencies in research data.
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits to ensure protocol compliance and data integrity. Additionally, you will collaborate with investigators and site staff while managing study documentation and resolving data queries.
The specialist is responsible for processing customer care tasks, including loan document fulfillment, incoming mail, and system updates. They also handle ACH requests, verification of mortgage inquiries, and the generation of standard payoff statements.
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The Global Study Manager acts as the primary liaison between clients, CROs, and internal teams to ensure seamless study delivery. They provide project management oversight, including budget, risk, and milestone management for a portfolio of global and local clinical studies.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
You will build technical prototypes for AI verification and collaborate with external experts to translate research into practical policy tools. The role involves working across machine learning engineering, cybersecurity, and systems architecture to develop robust and auditable verification mechanisms.
The Clinical Research Associate II acts as the primary contact for clinical sites, ensuring study protocol adherence, data integrity, and regulatory compliance. They are responsible for managing site relationships, conducting monitoring visits, and overseeing study documentation throughout the trial lifecycle.
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