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Develop and lead an integrated content and research strategy for HR and talent professionals, producing editorial content, research publications, learning programs, and conference and webinar programming. Represent the organization as a subject-matter expert, build relationships with practitioners and speakers, support leadership councils, and lead a collaborative team while improving audience engagement.
Participants will engage in online surveys, focus groups, and product testing to provide feedback on various services and products. They are responsible for completing their panel profile to receive relevant study invitations.
The Clinical Research Associate is responsible for managing site relationships, ensuring protocol compliance, and overseeing the quality and integrity of clinical trial data. They conduct various site visits, including qualification, initiation, monitoring, and termination, while protecting the rights and well-being of trial subjects.
Build historical financial models and conduct company, industry, and macroeconomic research to support investment theses and recommendations. Develop client and industry relationships, prepare research reports and presentations, and collaborate across products to strengthen analysis and corporate access.
The Director of Research will lead and scale the Beeck Center's applied research portfolio, focusing on digital transformation and public service delivery. They are responsible for defining strategic research directions, managing cross-functional teams, and translating practitioner insights into actionable policy recommendations.
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Conduct and oversee clinical trial site monitoring, including qualification, initiation, interim, and close-out visits, while ensuring protocol, GCP, regulatory, and quality compliance. Guide and mentor CRA colleagues, resolve site and study issues, support trial documentation and reporting, and coordinate with sponsors and cross-functional teams.
The consultant will conduct qualitative research, including in-person interviews and observations in West Kalimantan, to capture the experiences of program participants. They are responsible for transcribing data, analyzing findings, and drafting a 3,000-word article that highlights the program's impact and participant challenges.
Lead end-to-end quantitative research engagements, including study design, fieldwork, analysis, and reporting for technology and gaming clients. Act as a strategic advisor to clients while managing multiple complex projects and supporting business development efforts.
Conduct and oversee clinical trial site monitoring, including site visits, source data verification, regulatory documentation, investigational product accountability, and adverse event reporting. Guide and mentor CRA colleagues, support study planning and budgets, resolve site issues, and ensure compliance with protocols, ICH GCP, regulations, and SOPs.
The Research Computing Services Manager provides technical and financial oversight for non-desktop computing infrastructure to support biomedical research. They lead teams across Linux, Windows, database, and storage domains to ensure efficient, secure, and reliable research operations.
The Senior Director leads a team of Account Managers to drive retention and growth across a $60M+ research program portfolio. They are responsible for managing renewal strategies, coaching staff on complex negotiations, and collaborating cross-functionally to improve partner outcomes.
The Contract Clinical Research Associate manages clinical study sites to ensure adherence to GCPs, SOPs, and regulatory requirements. They perform site monitoring visits, track subject recruitment, and maintain essential study documentation throughout the trial lifecycle.
Conduct original research in generative AI and large language models applied to crypto and financial domains, focusing on reasoning under market uncertainty and multi-agent coordination. Design and execute rigorous experiments to develop novel post-training methodologies and evaluation frameworks for LLMs in adversarial financial environments.
Conduct in-depth research and risk assessments of various crypto projects to provide holistic insights. Analyze market trends and synthesize data from multiple sources to support informed decision-making.
The Research Analyst will conduct due diligence on issuers and partners while building commercial and financial models to evaluate product structures. They will also produce research memos and presentations to support key commercial decisions and track equity capital market developments.
The Clinical Research Associate performs on-site and remote monitoring activities to ensure investigational sites are adequately prepared and compliant. They are responsible for training site staff and supporting regulatory or ethics committee submissions.
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The Clinical Research Associate conducts site monitoring visits, ensures protocol compliance, and provides leadership in the management and execution of clinical trials. They also collaborate with cross-functional teams to resolve site issues, manage study budgets, and maintain data integrity through source document verification.
The Clinical Research Associate conducts site monitoring responsibilities to ensure clinical trial compliance, quality, and adherence to protocols. They provide leadership and guidance to the team while managing site relationships, data integrity, and regulatory documentation.
The Clinical Research Associate conducts site monitoring visits, ensures protocol compliance, and provides leadership in the management and execution of clinical trials. They also collaborate with cross-functional teams to resolve site issues, manage study budgets, and maintain data integrity through meticulous source document review.
The Research Scientist will enhance the reasoning and planning capabilities of foundation models throughout the development lifecycle, including data synthesis and reinforcement learning. They will also design evaluation methodologies and build multi-agent systems to solve complex real-world problems.
The role involves producing high-quality grant applications for charitable organizations and researching suitable funding opportunities. You will also be responsible for managing application deadlines and utilizing AI tools to improve research and writing efficiency.
You will coordinate clinical monitoring and site management processes to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. Responsibilities include conducting site visits, verifying data accuracy, managing documentation, and resolving site-related issues to ensure subject safety and data reliability.
The analyst will work across all aspects of data, from engineering and building machine learning models to creating sophisticated visualizations. They are responsible for analyzing large volumes of transactional and operational data to provide actionable recommendations for executives.
Contribute to the design and execution of experiments in reasoning model training and post-training alignment within financial contexts. Collaborate with engineering teams to translate research findings into production systems for a 24/7 trading environment.
Manage and execute full-service custom quantitative and qualitative research studies from kickoff to final presentation. Synthesize complex data into strategic, actionable narratives that drive decision-making for major brand clients.
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The Clinical Research Associate is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. They also collaborate with investigators to facilitate study conduct and perform data review to maintain high-quality clinical data.
The research resident will conduct rigorous quantitative and qualitative analysis on emerging AI and biosecurity risks to inform policy and public good. They will communicate findings to both technical and non-technical audiences through policy briefs and detailed research reports.
Manage clinical research activities at investigative sites, including site selection, study start-up, and conducting various monitoring visits. Ensure protocol adherence, regulatory compliance, and high-quality data collection while providing leadership and support to site personnel.
Perform clinical monitoring activities including site qualification, initiation, and close-out visits for various clinical trials. Manage investigative sites, ensure data integrity and patient safety, and maintain accurate documentation in accordance with study protocols.
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