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Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
The specialist reviews, drafts, and negotiates non-funded research agreements such as NDAs, MTAs, and DUAs with external partners. They ensure all contracts align with University policies, regulatory requirements, and risk-management standards while advising faculty on contractual implications.
The role focuses on identifying new organizations and generating leads through market research and targeted outbound outreach. The specialist will manage leads in a CRM and collaborate with the team to refine messaging and evaluate training needs for clinical research sites.
The VP of Research will lead the intelligence direction of the system, defining how AI reasons, evaluates, and improves. They will oversee model architecture decisions, evaluation frameworks, and the overall alignment and safety strategy.
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The Research Associate will conduct research on higher education policy and social stratification using large-scale administrative data. Responsibilities include data management, producing scholarly publications, and collaborating on grant writing and project management.
Develop and execute targeted research strategies to identify and engage passive executive talent within the biopharmaceutical industry. Provide advanced market analysis, talent mapping, and strategic advisory to Client Partners and Recruiters.
Coordinate day-to-day remote clinical trial operations and facilitate remote patient visits. Manage data entry in EDC and CTMS systems while serving as a virtual liaison between sponsors and CROs.
Identify, qualify, and schedule potential participants for Central Nervous System clinical research studies through inbound and outbound calls. Document all interactions in recruitment systems while ensuring compliance with IRB and HIPAA regulations.
The role focuses on building targeted prospect databases and identifying key decision-makers across multiple industries. It involves managing outbound email and LinkedIn campaigns and conducting telephone prospecting to schedule meetings.
Support medical writing and safety monitoring teams through QC review of regulatory documents and data verification of statistical outputs. Manage document e-publishing, archiving, and provide secretarial support for DMC/DSMB meetings.
Design and implement next-generation AI agents and post-training methods like RLHF and GRPO to align models with real-world workloads. Act as a technical bridge between customers and research teams to translate applied data into product and research priorities.
The role involves conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Additionally, the CRA will perform data review and collaborate with investigators to maintain high-quality clinical data.
Manage the full lifecycle of international healthcare market research projects to ensure client satisfaction and financial goals are met. Lead and mentor junior project managers while optimizing internal processes and maintaining ISO accreditation standards.
Develop and integrate novel AI algorithms and models to augment physics-driven simulation systems for space sustainability. Collaborate with cross-functional teams to build mission-critical decision-support tools and contribute to technical research publications and patents.
The specialist provides comprehensive support for the institution's research compliance program through monitoring, auditing, and education. They are responsible for developing human research protections training and ensuring adherence to federal regulations and institutional policies.
The specialist provides comprehensive support for the institution's research compliance program through monitoring, auditing, and education. They are responsible for developing human research protections training and ensuring adherence to federal regulations and institutional policies.
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Provide clinical training, technical assistance, and consultation regarding substance use prevention and intervention within early psychosis care. Collaborate with stakeholders to integrate feedback and research to improve clinical outcomes and program delivery.
Conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Collaborate with investigators and perform data review to maintain high-quality clinical data and study documentation.
Oversees the execution of clinical trials at investigative sites, acting as a liaison between the sponsor and sites to ensure data integrity and participant safety. Responsibilities include site initiation, monitoring, close-out, and mentoring junior staff.
The CRA is responsible for managing the full lifecycle of clinical sites, including qualification, initiation, monitoring, and close-out visits. They ensure protocol adherence, verify source documents for data veracity, and manage site documentation within the Trial Master File.
The CRA is responsible for the full lifecycle of site management, including qualification, initiation, monitoring, and close-out visits. Key duties include verifying source documents, ensuring protocol adherence, and managing Trial Master File documentation.
Participate in research studies to contribute to meaningful outcomes. Perform data entry tasks and follow instructions to earn income from home.
Manage research activities at clinical sites, including site identification, start-up activities, and study maintenance. Conduct site initiation visits and ensure compliance with regulatory requirements and safety reporting.
Define and evolve the segment strategy for grant-funded life science markets, including academia and government institutions. Translate portfolio priorities into clear positioning and value propositions to guide marketing and commercial execution.
Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to SOPs and GCP. Maintain site correspondence, complete visit reports, and oversee clinical research data and patient charts.
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Responsible for the full lifecycle of site management, including qualification, initiation, monitoring, and close-out visits. The role involves ensuring protocol adherence, verifying source documents, and mentoring less experienced CRAs.
The role involves conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Additionally, the CRA will perform data review and collaborate with investigators to maintain high-quality clinical data.
The analyst is responsible for researching and monitoring global exchange regulations to maintain and improve client reports on the Global Exchanges portal. They will conduct stock market due diligence, publish regulatory articles, and oversee shareholder disclosure solutions.
Build and maintain agentic research infrastructure, automated analysis pipelines, and distributed training systems. Partner with researchers to scale experiments to frontier-tier models and translate theoretical insights into empirical tools.
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