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The Clinical Research Manager is responsible for the end-to-end performance and project management of assigned clinical protocols in compliance with ICH-GCP and regulatory standards. They serve as the main point of contact between Country Operations and clinical trial teams, ensuring deliverables are met from feasibility through to study close-out.
The Research Analyst Engineer is responsible for researching, gathering, and organizing technical hardware and software specifications for internal databases. They also perform fact-checking, content editing, and ensure all web publications meet quality and tone guidelines.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with SOPs and regulatory requirements. They will manage investigational product accountability, oversee unblinded site activities, and ensure data quality and protocol compliance.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with company SOPs and regulatory requirements. They will manage investigational product accountability, oversee unblinded site activities, and ensure data quality and protocol compliance throughout the study.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with SOPs and regulatory requirements. They will provide unmasked support for ophthalmology studies, ensuring data integrity, subject safety, and protocol compliance.
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You will support the management of clinical trial sites in compliance with ICH-GCP and study protocols while participating in site initiation, monitoring, and close-out visits. Additionally, you will conduct source data verification and assist cross-functional teams in ensuring data quality and patient safety.
The Clinical Research Associate is responsible for conducting site visits, ensuring protocol compliance, and maintaining data integrity throughout clinical trials. They also collaborate with investigators and site staff to facilitate study conduct and contribute to the preparation of study documentation.
The Principal, Market Research Scientist serves as the organization's expert on quantitative research methodology, establishing analytical standards and best practices. They advise research teams on study design, sampling, and statistical approaches while mentoring staff and representing the company's expertise to clients.
The Legal Associate will draft and review contracts, conduct legal research, and manage legal documentation. They will also provide general administrative support while ensuring compliance and effective communication within the team.
The Registered Dietitian will conduct virtual lifestyle counseling visits for clinical trial participants to improve nutrition and mental health outcomes. They will also coordinate with site personnel to ensure accurate documentation and adherence to study protocols.
The Registered Dietitian will conduct virtual lifestyle counseling visits for clinical trial participants to improve nutrition and health habits. They will also coordinate with project managers to ensure accurate documentation and adherence to study protocols.
The Research Project Coordinator will administratively manage research protocol implementation and ensure efficient logistical execution of study activities. Responsibilities include data collection, record management, budget oversight, and providing regular updates on protocol status to the research team.
The research scientist will lead efforts to discover insights regarding AI capabilities and proclivities using existing data and infrastructure. They will also scale the AI Village project to demonstrate long-horizon agentic capabilities and study emergent model behaviors.
The Research Assistant will support the design and execution of research projects, transforming raw data into business-ready insights for global clients. They will also leverage AI tools to accelerate research workflows while maintaining rigorous human oversight and methodological integrity.
Manage federal, state, and private research grants and contracts to ensure compliance with grantor requirements. Support the organization's mission by providing accurate financial accounting for designated research funds.
You will build and manage the post-training infrastructure, including synthetic data pipelines, model evaluation frameworks, and training environments. You will also be responsible for shipping models into production and continuously improving their performance for voice and text agents.
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The Director will oversee the strategic planning, budget management, and implementation of research and student engagement programs for the Emory Policy Institute on Countering Antisemitism. This role involves coordinating fellowships, internships, and academic programming while serving as a primary liaison between students, faculty, and external policy partners.
Lead computerized system validation activities for regulated digital and AI applications throughout the software development lifecycle. Partner with cross-functional teams to ensure systems meet business requirements, regulatory standards, and quality expectations.
The Junior Clinical Research Associate is responsible for conducting site visits, including pre-study, initiation, monitoring, and termination. They also ensure adherence to regulatory standards, perform source document verification, and manage data validation and query resolution.
The IT Manager oversees the IT Business Solutions groups, providing leadership and guidance to ensure the effective delivery of network infrastructure, hardware, and software services. They are responsible for executing departmental strategies, managing team performance, and solving complex technical and operational problems.
The analyst will conduct quantitative analyses on patient datasets and harmonize data from multiple sources to support research questions. They will also translate these analytical findings into scientific communications such as white papers, abstracts, and marketing content for diverse audiences.
Conduct site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance and data integrity. Collaborate with investigators and site staff to facilitate study conduct and maintain high-quality clinical data.
The Associate Tax Research Specialist will research tax code changes and provide guidance to programmers for updating tax software calculations. They will also design test cases to ensure tax return accuracy and contribute to technical documentation and customer-facing guidance.
The Research Analyst will conduct primary and secondary research to identify market trends and visitor behaviors to support strategic marketing decisions. They are responsible for managing surveys, building data visualizations, and preparing technical reports for leadership.
The Sr. Research Analyst manages end-to-end research projects, including survey design, data collection, and the generation of defensible insights. They also partner with leadership to translate strategic priorities into research plans and communicate findings to internal and external stakeholders.
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The specialist will lead the design and implementation of rigorous research and evaluation efforts focused on economic mobility and human services programs. They will also provide strategic guidance to multidisciplinary teams and translate complex research findings into actionable insights for stakeholders.
The Research and Writing Attorney will conduct legal research and draft motions, briefs, and memoranda to support trial attorneys in personal injury cases. They will also collaborate with case teams to develop legal strategies and monitor developments in New Mexico case law.
The Research and Writing Attorney will conduct legal research and draft motions, briefs, and memoranda to support trial attorneys in personal injury cases. They will also collaborate with case teams to identify legal issues and strengthen case positions for settlement and trial.
The Senior Sponsored Research Administrator manages complex sponsored projects throughout the full lifecycle, from proposal development to award closeout. They serve as a primary resource for faculty, ensuring compliance with sponsor regulations and institutional policies while mentoring junior staff.
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