Discover the best remote jobs, online jobs, and work from home opportunities across 15+ categories. Find your ideal remote work position and start your work from home career today!
Trusted by 200,000+ remote workers worldwide.
The role involves supporting executive visibility through research, content repurposing, and managing speaking or partnership opportunities. You will also maintain databases, track application pipelines, and prepare briefing notes for the founder.
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Key tasks include monitoring clinical sites, resolving performance issues, and collaborating with cross-functional teams to ensure accurate data reporting.
The Senior Director will establish and lead the global HEOR and RWE strategy to demonstrate the value of Immatics' oncology therapies throughout their lifecycle. This role involves designing research studies, managing external data partners, and collaborating with cross-functional teams to support market access and regulatory objectives.
The Manager of Regulatory Affairs oversees all regulatory operations for site clinical operations and ensures full compliance with FDA and GCP guidelines. They are responsible for managing the regulatory department, developing compliance strategies, and coordinating relationships with industry sponsors and governmental auditors.
The Manager of Regulatory Affairs oversees all regulatory operations for site clinical operations and ensures full compliance with FDA and GCP guidelines. They are responsible for managing the regulatory department, developing compliance strategies, and fostering relationships with industry sponsors and government agencies.
We watch for new "Research" jobs and email you the matches. Free. Unsubscribe in one click.
The analyst will lead the implementation and support of Epic research applications, ensuring system architecture aligns with organizational needs. They are responsible for defining requirements, managing project lifecycles, and providing technical leadership to cross-functional teams.
The Research Director will own the learning agenda for Emergency Cash programs, setting research priorities and strategic impact evaluations. They will provide technical leadership, mentor staff, and represent the organization's research findings to external stakeholders.
Perform monitoring and site management to ensure clinical studies adhere to protocols, regulations, and sponsor requirements. Manage site practices, including recruitment planning, regulatory submissions, and data integrity.
The Senior Clinical Research Associate will conduct countrywide monitoring visits to ensure data integrity and patient safety at investigator sites. They are responsible for maintaining Trial Master Files and delivering quality monitoring reports in accordance with clinical monitoring plans.
You will research emerging threats and malware to produce insightful technical content such as blogs, whitepapers, and research reports. Additionally, you will collaborate with internal teams to translate platform capabilities into compelling narratives that resonate with the security community.
You will research emerging threats and translate findings into high-impact technical content to support the company's growth and market positioning. You will also collaborate with product and engineering teams to create compelling narratives that demonstrate the platform's technical depth.
The analyst will lead the firm's coverage of AI infrastructure financing by mapping capital flows and evaluating credit risks across the ecosystem. They will build quantitative models to assess collateral resilience and produce flagship research reports for financial institutions and investors.
The Clinical Research Coordinator ensures oversight and compliance of system-wide clinical research activities for the Retrospective Core. They are responsible for study management, data collection, data integrity, and safeguarding participant privacy in accordance with regulatory standards.
The Research Engineer Intern will develop and optimize compute kernels for AI hardware and improve inference performance for large language models. They will also build benchmarks, profile system performance, and contribute code to open-source AI infrastructure projects.
The Senior Clinical Research Associate will monitor clinical trials to ensure compliance with protocols and regulatory standards while managing site operations. They are responsible for conducting site visits, performing source document verification, and providing training to site staff.
The Clinical Research Associate will monitor clinical trial sites through on-site and remote visits while maintaining strong relationships with investigators and site staff. They are responsible for managing study documentation, ensuring compliance, and implementing corrective actions to maintain study integrity.
We watch for new "Research" jobs and email you the matches. Free. Unsubscribe in one click.
The Director of Operations is responsible for driving the growth, scalability, and operational consistency of the Remote Research Clinicians business. This role provides strategic leadership across client engagement, technology-enabled operations, and quality oversight to ensure delivery excellence.
You will conduct clinical trial monitoring activities, including site visits and data review to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and contribute to the preparation of essential study documentation.
The Research Scientist will design and implement computational workflows to investigate catalytic cycles, reaction mechanisms, and structure-selectivity relationships. They will also collaborate with interdisciplinary teams to develop large-scale datasets and machine learning models for homogeneous catalyst discovery.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and project teams.
The Research Coordinator will oversee day-to-day project management, including developing timelines, ensuring ethics compliance, and managing data collection logistics. They will also coordinate research activities such as chart audits, focus groups, and interviews while supervising research assistants.
Serve as the primary point of contact for investigational sites while conducting site visits to ensure compliance with ICH-GCP and regulatory standards. Manage site documentation, monitor patient safety, and oversee drug accountability to ensure high-quality clinical data.
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 collaborate with investigators and site staff while performing data reviews to maintain high-quality clinical documentation.
The Clinical Research Associate serves as the primary point of contact for investigational sites, conducting monitoring visits to ensure compliance with ICH-GCP and regulatory standards. They are responsible for maintaining clinical documentation, monitoring patient safety, and overseeing site-level recruitment and data integrity.
The Clinical Research Associate will manage site selection, activation, and regulatory compliance for clinical trials across various therapeutic areas. They will act as the primary point of contact for sites and study teams to ensure project milestones are met while maintaining high-quality documentation.
We watch for new "Research" jobs and email you the matches. Free. Unsubscribe in one click.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They perform risk-based monitoring, conduct site visits, and manage essential documentation to guarantee data reliability and subject well-being.
Lead the design and execution of scientific and clinical studies, with a focus on UAE-based collaborations and populations. Analyze complex physiological and wearable datasets to generate actionable health insights and contribute to scientific dissemination.
Deliver high-quality instruction in research and evidence-based practice while facilitating meaningful classroom discussions. Support program initiatives and maintain compliance with accreditation standards while modeling the university's mission.
The administrator manages sponsored programs, including budget preparation, financial reporting, and ensuring compliance with university and funding guidelines. They also supervise staff, oversee labor distribution, and implement process improvements to support research administration.
Stop the endless job search. Our AI finds and applies to the best jobs for you.
Everything you need to know about remote work
