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Manage research activities at clinical sites, including site identification, start-up, and close-out. 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.
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 identification, start-up, maintenance, and close-out phases. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
The Senior CRA manages clinical investigative sites for Phase I-IV pharma trials, ensuring data quality and adherence to ICH/GCP and company SOPs. Key duties include performing site initiation visits, continuous monitoring, and collaborating with internal stakeholders to resolve data queries.
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The Senior CRA manages clinical investigative sites for Phase I-IV pharma trials, ensuring data quality and adherence to ICH/GCP and company SOPs. Key duties include performing site initiation visits, continuous monitoring, and collaborating with internal stakeholders to resolve data queries.
The intern will conduct AI SaaS market mapping and ICP research to identify high-fit accounts and buyers. They will prepare outbound strategies and company briefs to support founder-led sales and customer acquisition.
Develop and validate novel methods for modeling complex interconnected systems at the intersection of graph theory and machine learning. Collaborate with engineering and clinical experts to transition research findings into production and publish results that advance the field.
Conduct rigorous applied research on water, climate, and equity using mixed methods to produce high-quality reports and peer-reviewed publications. Coordinate project workflows, support fundraising activities, and collaborate with external partners to advance climate resilience in frontline communities.
Perform competitive intelligence, landscape, and patentability searches to support global patent procurement and enforcement. Collaborate with scientists and attorneys to analyze findings and inform exclusivity and freedom to operate strategies.
The Clinical Research Lead drives the execution of clinical trials through strategic investigator engagement and site performance management. They serve as a scientific ambassador to ensure protocol understanding and co-develop enrollment strategies to optimize trial delivery.
Perform clinical monitoring and site management to ensure trial conduct aligns with protocols, ICH-GCP guidelines, and regulatory requirements. Conduct remote and on-site visits to assess compliance, manage documentation, and maintain audit readiness.
The CRA II is responsible for monitoring investigator sites to ensure protocol compliance, data reliability, and subject safety. This includes conducting on-site and remote visits, managing essential documentation, and maintaining relationships with clinical sites.
Perform and coordinate all aspects of clinical monitoring and site management to ensure protocol and regulatory compliance. Conduct remote and on-site visits to assess data reliability and maintain audit readiness for oncology trials.
Oversee and manage Phase II–IV clinical trials to ensure compliance with protocols, regulatory requirements, and industry standards. Conduct site visits and collaborate with cross-functional teams to ensure data integrity and patient safety.
Responsible for the fiscal coordination of local, federal, state, and private grants and contracts. Liaises with Corporate Finance and the Foundation to ensure compliance with government regulations and agency requirements.
Design and lead original research studies by developing methodologies and analyzing large datasets to create compelling data narratives. Collaborate with cross-functional teams to build BI dashboards and translate findings into strategic business recommendations for B2B clients.
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The Research Development Strategist collaborates with faculty to develop funding proposals and launch new research initiatives. The role involves identifying funding opportunities and nurturing partnerships between UTMB and other institutions.
Lead and oversee clinical trial activities at a country or regional level, focusing on mentorship, oversight, and consistency in monitoring practices. Coordinate cross-functional teams to ensure high-quality execution, compliance, and timely delivery of study milestones.
The Senior Research Associate leads research analysis projects focused on the teacher labor market and compensation reforms. Responsibilities include designing experiments, leading data collection, and writing academic papers and grant reports.
The Research Assistant will oversee data collection, organization, and management for HIV implementation science studies. Responsibilities include running statistical models, cleaning data, and preparing reports and publications to support the PI.
Drive sustainable territory growth by developing new business and expanding existing accounts within the Waters Biosciences division. Act as the strategic owner of the Florida region, aligning customer needs with integrated solution-based value across the portfolio.
Lead the UX research function by defining the research roadmap and identifying critical knowledge gaps to influence company-level decisions. Partner with cross-functional leads to execute generative, formative, and summative research while mentoring the user research team.
The Research Fellow will drive complex research projects focused on the extraction, normalization, and ingestion of civic data. They will also manage remote researchers and contractors to ensure accurate and timely data delivery.
Lead independent research projects in sequence and generative modeling to advance the state of the art in audio and music. Design rigorous experiments and publish findings at top-tier AI venues while collaborating with engineering teams to improve Smule's products.
Develop and adapt state-of-the-art ML techniques to solve product challenges in audio processing, recommendation, and generative music. Design rigorous experiments and build prototype models to improve user experience and product quality.
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Design and maintain research infrastructure, including distributed training pipelines and evaluation frameworks. Collaborate with scientists to optimize model architectures and ensure the reproducibility of research results.
Independently monitor Phase II-IV clinical trials to ensure compliance with ICH-GCP and regulatory requirements. Manage site visits, study documentation, and collaborate with cross-functional teams to ensure patient safety and data quality.
Independently monitor Phase II–IV clinical trials to ensure compliance with ICH-GCP and regulatory requirements. Manage site qualification, initiation, and close-out visits while ensuring data integrity and patient safety.
Manage and independently monitor Phase I-III clinical trials for biotech sponsors in the Netherlands to ensure regulatory compliance. Conduct site visits and manage study documentation, regulatory submissions, and ethics approvals while collaborating with cross-functional teams.
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