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The Clinical Research Associate oversees the operational aspects of clinical trials at investigational sites to ensure data integrity and regulatory compliance. They are responsible for monitoring site performance, managing trial materials, and facilitating communication between sponsors and site personnel.
The Senior Tax Research Analyst conducts in-depth research on complex federal and state tax matters to provide well-reasoned technical guidance and documentation. They also coordinate project team activities, develop training materials, and ensure compliance with research standards across the organization.
Scholars will own end-to-end safety research projects, from formulating hypotheses to implementing evaluation harnesses and conducting controlled experiments. They will work under mentor guidance to drive day-to-day research, analyze results, and produce reproducible technical outputs.
The interventionist will deliver individual telehealth sessions for a multi-site cancer rehabilitation study, including cancer survivorship education and goal-setting. They are also responsible for documenting session content and timing within a REDCap database while adhering to study protocols.
Manage research projects, including study design, data collection and analysis, internal team coordination, and supervision of research staff and interns. Contribute to grant proposals, interpret quantitative and qualitative findings, and help prepare reports, manuscripts, and conference abstracts in collaboration with investigators and community partners.
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Lead the design and execution of retrospective outcomes research for biopharma clients, developing innovative methods and translating complex real-world and multimodal data into rigorous, actionable evidence. Guide scientific publications and client strategy, partner across data science, biostatistics, and product teams, ensure regulatory and ethical quality, and manage a team of outcomes research scientists.
Research markets, competitors, customers, partners, and business opportunities, and organize relevant information to support growth initiatives. Develop business development materials and presentations, participate in meetings, and collaborate on projects while delivering accurate work on time.
Support clinical trial sites from study start-up through closeout by conducting site visits, training site staff, and monitoring protocol compliance, data quality, and Good Clinical Practice requirements. Maintain study documentation and investigational product records, review adverse event reporting, assess site performance, and communicate monitoring findings and corrective actions.
Manage assigned clinical trial sites throughout study start-up, conduct, and close-out, ensuring compliance with protocols, ICH-GCP, regulations, and company procedures. Monitor site performance and data quality, support recruitment and site development, maintain study documentation and systems, and mentor junior CRAs.
Lead complex research initiatives from strategy and study design through execution, synthesis, storytelling, and activation of insights. Advise cross-functional partners, establish research standards, and guide researchers through coaching, prioritization, and development.
Edit, refine, and occasionally write research, thought leadership, marketing, and promotional content for institutional finance audiences, ensuring accuracy, clarity, brand consistency, and SEO optimization. Manage editorial workflows and calendars, coach writers, collaborate with cross-functional teams, and use content performance insights to improve published materials.
Build and optimize inference systems for Prime Intellect’s reinforcement-learning research, including support for new model architectures, long-horizon agent rollouts, and multi-node mixture-of-experts inference. Improve throughput, weight-update efficiency, and numerical reliability while collaborating with researchers on inference-efficient model architectures.
Find and process web, code, and technical data into high-quality, training-ready corpora, with scalable pipelines and clear provenance and versioning. Collaborate with researchers to design data mixtures and run controlled experiments that measure how data choices affect pretraining, reasoning, coding, and long-context model performance.
Develop pretraining code and take model experiments through full-scale training runs, evaluating architecture changes and improving throughput and resilience. Investigate training dynamics, run reproducible ablations, and collaborate on data mixtures, midtraining, and long-context experiments.
Design and implement challenging coding and long-horizon agent tasks, executable environments, evaluation systems, and scoring logic for training and assessing Prime Intellect models. Build and curate RL data pipelines, investigate model and harness failures, and collaborate with researchers to test whether task and data changes improve performance on held-out tasks.
Participate in a moderated remote usability session with a UX researcher, describing how you send money from the UK to India. Complete an approximately $20 transfer using the test application and share your reactions and feedback aloud during the process.
Develop and evaluate reinforcement learning algorithms and training systems for open models, including methods for reasoning, coding, and long-horizon tasks. Design scaling experiments, improve the prime-rl framework, and diagnose stability, performance, and numerical issues across training and rollout systems.
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Lead scientific work across research projects and author, review, and finalize client deliverables such as protocols, reports, analysis plans, evidence dossiers, presentations, and manuscripts. Manage project scope, timelines, budgets, and staffing; engage with clients; mentor junior staff; and contribute to proposals, conferences, training, recruitment, and regulatory meeting preparation.
Lead and oversee a portfolio of research projects, ensuring scientific quality, timely delivery, and adherence to contracted budgets while presenting findings in peer-reviewed journals and at professional meetings. Provide scientific leadership and mentorship to junior staff, delegate project tasks, and develop client relationships and business opportunities.
Advise customers on research objectives, methodology, sampling, and study design, and manage research engagements from scoping and setup through data collection, quality assurance, analysis, and reporting. Lead client conversations and collaborate with Sales, Customer Success, Product, and Supply teams to deliver actionable insights and improve research processes.
Audit existing lifecycle journeys and tools, identify activation and retention gaps, and prioritize improvements with Growth Marketing, Product, and Customer Success. Build and launch email and in-app onboarding, retention, reactivation, and expansion programs; define PQL signals, run experiments, report results, and document processes.
Participate in paid online or video focus groups, surveys, and at-home product tests. Share feedback on advertisements, apps, services, and products.
Monitor Phase I–IV oncology clinical trials and manage site activities from start-up through close-out, ensuring compliance with study protocols, GCP/ICH guidelines, and regulatory requirements. Train site personnel, oversee documentation and investigational product accountability, resolve data queries, maintain site communications, and prepare monitoring reports.
Leads Quva Pharma’s enterprise R&D strategy and product portfolio, overseeing development from clinical and regulatory assessment through formulation, validation, technology transfer, launch, and lifecycle improvement. Builds and leads a multidisciplinary R&D organization, coordinates cross-functional programs, and ensures development work is compliant, inspection-ready, and aligned with clinical, operational, and commercial priorities.
The counselor will provide intervention sessions to study participants and coordinate appointments while ensuring adherence to research protocols. They are also responsible for maintaining accurate documentation and providing support to participants experiencing crises.
The position manages the full lifecycle of sponsored grants and contracts, including budget establishment, financial reconciliation, and reporting. It also serves as a primary resource for faculty and principal investigators regarding financial compliance and administrative requirements.
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The intern supports site-level activities including feasibility, site activation, regulatory compliance, and site support throughout the clinical research lifecycle. They collaborate with project leadership to ensure study milestones are met while maintaining high-quality documentation and audit readiness.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence and manage documentation throughout the clinical trial lifecycle.
The Clinical Research Associate monitors investigator sites using a risk-based approach to ensure data accuracy, regulatory compliance, and protocol adherence. They also manage site initiation, trial close-out, and maintain regular communication with investigative teams to resolve issues.
Research frontier AI systems and develop datasets, experiments, prototypes, tools, and evaluation frameworks across areas such as reinforcement learning, post-training, synthetic data, and AI agents. Analyze results rigorously and collaborate across teams to turn validated research into scalable products and share findings with the research community.
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