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The Senior Clinical Research Associate leads multi-center clinical research studies, performing site monitoring visits and ensuring compliance with protocols and regulatory standards. They also provide mentorship to junior team members, manage study metrics, and oversee site activation and data reporting processes.
This role assists in the development and execution of clinical evidence generation strategies and clinical study activities for the Gastrointestinal Solutions Division. Responsibilities include writing study protocols, managing regulatory submissions, and collaborating with cross-functional teams to support product commercialization.
The Technical Advisor will conduct epidemiological analysis, model program impact, and evaluate cost-effectiveness to support strategic health system decisions. They will also translate complex analytical findings into clear outputs for senior leadership and philanthropic funders.
The role involves managing client relationships and project delivery for connected devices within clinical research. Responsibilities include developing departmental strategy, overseeing quality control, and ensuring compliance with regulatory guidelines.
You will lead the development of detection capabilities and AI workflows to enhance Elastic Security's threat research and defense mechanisms. This involves investigating multidomain threat vectors and presenting findings to improve team knowledge and community awareness.
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The Postdoctoral Research Fellow will independently design, execute, and interpret complex molecular, cellular, and animal-based studies focused on musculoskeletal regeneration. Additionally, the fellow will contribute to the laboratory's mission by writing manuscripts, applying for grants, and mentoring research staff.
The role involves managing pre-award activities for a portfolio of grants and contracts, including proposal development, budget preparation, and ensuring compliance with sponsor and institutional guidelines. It also includes providing strategic guidance to investigators and coordinating workload distribution for a team of specialists.
Conduct site qualification, monitoring, and close-out visits while ensuring protocol compliance and patient safety. Collaborate with site staff to manage clinical data and contribute to the preparation of study documentation and reports.
The Senior Clinical Research Associate is responsible for managing investigative sites and performing monitoring activities to ensure data integrity and subject safety throughout the clinical trial lifecycle. They will facilitate communication between the client and sites, oversee regulatory compliance, and support site activation and close-out processes.
The associate will engage in client-facing project work, including project management, intensive data analysis, and the creation of compelling presentations. They will help clients achieve organizational effectiveness, improve student outcomes, and implement new technologies.
The Senior Clinical Research Associate monitors and oversees clinical trials at client sites to ensure data quality, integrity, and regulatory compliance. They also manage site-specific activities, including feasibility, qualification, and the resolution of site-related issues throughout the trial lifecycle.
The Senior CRA will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and industry standards. Responsibilities include conducting site visits, resolving performance issues, and collaborating with cross-functional teams to ensure accurate data collection.
The Senior CRA will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and GCP standards. Responsibilities include conducting site visits, resolving performance issues, and collaborating with cross-functional teams to ensure accurate data reporting.
The Senior CRA will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Responsibilities include monitoring clinical sites, resolving performance issues, and collaborating with cross-functional teams to ensure accurate data collection.
This role involves performing remote and on-site monitoring visits to ensure clinical trial compliance and data accuracy. The associate also manages operational aspects of clinical sites, including site activation, document maintenance, and serving as a primary liaison for study personnel.
The Lead Clinical Research Associate provides leadership, oversight, and mentorship for regional clinical trials while collaborating with project teams to ensure high-quality study execution. This role focuses on remote monitoring oversight, compliance, and data integrity rather than direct site management.
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The Senior Clinical Research Associate will conduct on-site monitoring visits, manage site communications, and ensure data quality and compliance for clinical research projects. They will also oversee study timelines, support regulatory submissions, and act as a primary point of contact for project stakeholders.
You will conduct market and competitive research, audit marketing experiences, and analyze data to support client strategies. Additionally, you will manage timelines across concurrent engagements and ensure all deliverables meet high standards of accuracy and quality.
The analyst is responsible for conducting market and competitive research, auditing marketing experiences, and synthesizing data into actionable strategic reports. They manage timelines across multiple concurrent engagements while ensuring all deliverables meet high standards of accuracy and quality.
The Research Assistant supports the Research and Evaluation Portfolio by assisting with community-based research projects and engagements. They collaborate with staff to prepare reports, toolkits, and information packages while gathering data using Indigenous methodologies.
The Manager of Threat Research will lead a team dedicated to detecting compromised systems and expanding victim intelligence capabilities. They will own malware triage workflows, mentor researchers, and partner with product and engineering teams to translate telemetry into scalable features.
The intern will provide research, writing, and editing support for knowledge products related to impact investing and SDG financing. They will also assist in designing initiatives, preparing communication materials, and managing online content across social media channels.
The analyst supports project execution by researching policies and technical documentation to inform software user interface design and lifecycle management. They coordinate with cross-functional stakeholders to translate regulatory requirements into actionable inputs and develop operational sustainment strategies.
The Clinical Research Associate 2 is responsible for site management, monitoring activities, and ensuring compliance with regulatory requirements and SOPs. They coordinate site selection, manage trial documentation, and support recruitment efforts to ensure successful trial execution.
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will perform data review, resolve queries, and contribute to the preparation of study documentation and clinical reports.
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The Senior Clinical Research Associate manages site monitoring and relationship activities across multiple clinical studies to ensure high-quality execution and regulatory compliance. They also provide mentorship to less experienced staff and proactively identify and resolve operational issues to meet study objectives.
The Clinical Research Associate will conduct qualification, initiation, monitoring, and close-out visits to ensure patient safety and data integrity. They are also responsible for supporting site activation, maintaining accurate documentation, and building strong relationships with investigators.
The Research Administrator II independently manages the administrative and financial components of sponsored projects, including large-scale and complex awards. They support principal investigators throughout the award lifecycle, from proposal budget development to award setup, compliance monitoring, and project closeout.
Design and implement mathematical optimization models to solve complex industrial problems like scheduling and resource allocation. Collaborate with cross-functional teams to integrate these models into scalable production systems using Python.
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