Research Analyst

• Develop and maintain research for the Global X research library, including written reports, presentations, charts, videos, and other client-facing content.
• Monitor commodity markets and macroeconomic developments to produce timely commentary and market updates.
• Explain commodity market fundamentals, futures market dynamics, and ETF implementation in a clear, practical manner.
• Develop educational content covering ETF structure, index methodologies, portfolio construction, and competitive positioning.
• Conduct research projects supporting existing ETFs and potential new product development.
• Collaborate with Product, Capital Markets, Investment Strategy, and Sales teams on product positioning and market analysis.
• Respond to client and internal inquiries regarding ETF methodology, performance drivers, commodity fundamentals, and market developments.
• Present research through webinars, client meetings, conferences, podcasts, and media interviews.
• Support strategic initiatives across the Research team as needed.

AVP, Research Analyst

• Schedule and perform on-site or remote monitoring visit activities, inclusive of the following study visit types: Site Initiation Visit (SIV), Interim Monitoring Visit (IMV) / Routine Monitoring Visit (RMV), and Close Out Visit (COV).
• Contribute to the development of protocols, study tools, materials, and documentation for clinical sites.
• Provide feedback to assist sites with resolution of detected deficiencies and corrective action needed.
• Review site-level investigational drug accountability and safety event documentation.
• Review and verify patient files and records, informed consent, case report forms, and source documents for completeness, accuracy, consistency, and compliance; identify deficiencies; provide training and/or initiate corrective action as required.
• Identify, document, track, and report site protocol deviations and violations as defined within the EAP Monitoring Plan.
• Manage query resolution.
• Provide mentoring, training, and co-monitoring of junior team members.
• Assist in the development of applicable WEP Clinical Standard Operating Procedures.
• Develop applicable document templates, including (but not limited to), Monitoring Plans, Monitoring Visit Reports, Confirmation Letters, Follow-Up Letters, and Query Logs.
• Complete, review, and/or submit monitoring reports and query logs.
• Address protocol or monitoring-related questions received from clinical sites for assigned programs.

Clinical Research Associate

• Act as a project manager for the Research product
• Gain deep familiarity with our Research systems and liaise with various stakeholders
• Provide editorial review of the Research product, including from non-native speakers
• Ensure views are communicated clearly and reports are logically consistent
• Mitigate reputational risk by editing for tone and language
• Work with Compliance as needed
• Consistently apply corporate branding and style guidelines

Editor – Research Operations Analyst

• Lead the design and execution of market research projects
• Analyze and report on market research projects
• Deliver actionable insights utilizing various brand measurement sources
• Provide ongoing consumer research expertise and consultation to internal partners

Principal Associate, Market Research

• Collaborating with Leaders in Product Management, UX Design, and Engineering, to define the long-term vision and strategy for user experience research for the segment, aligning it with business objectives and goals.
• Provide close partnership for senior business stakeholders and development heads to deliver world-class experiences through data driven decision making
• Partner with Product Managers to understand business goals and objectives both at the portfolio and product level.
• Lead the planning and execution of user research initiatives, employing a variety of generative and evaluative research methods.
• Plan and execute generative and evaluative studies of various complexities and methodology.
• Partner with embedded UX design leads/teams to evaluate prototypes and solutions with customers
• Ensure Product teams gain a deep understanding of user needs, behaviors, and motivations.
• Ensure that the product teams are using research findings, data and insights to inform design decisions and validate design solutions.
• Drive the culture of feedback and metrics to drive continuous improvement in the user experience.
• AI Analysis: Use AI‑assisted data analysis techniques to accelerate synthesis of qualitative and quantitative research data (e.g., clustering themes, identifying patterns across large datasets, and surfacing emerging signals).
• Apply AI‑supported persona development and segmentation approaches to generate and evolve evidence‑based user archetypes grounded in behavioral, attitudinal, and contextual data.
• Contribute to the exploration and use of AI‑enabled journey mapping and experience modeling approaches (e.g., scenario simulation, agent‑based representations, or dynamic journey artifacts) to help product teams reason about complex, multi‑step user workflows.
• Partner with Product, Design, and Data Science to evaluate and shape the use of AI systems that support research operations, customer intelligence, and experience measurement.
• Critically assess AI‑generated insights for bias, validity, explainability, and alignment with user needs, regulatory constraints, and ethical design principles.
• Provide guidance to stakeholders on where AI meaningfully enhances research and decision‑making—and where human‑led research remains essential.
• Stakeholder management: Collaborating with cross-functional teams, including product managers, developers, and stakeholders, to ensure alignment and a shared understanding of user experience goals.
• Regular, transparent communication of status and metrics to management and stakeholders
• Advocate for, and actively implement, standard processes to ensure quality and consistency of work, and a joined-up approach for all teams in the business group/division.
• Involve all members of cross-functional teams in research and analysis
• Industry awareness: Staying up to date with the latest trends, technologies, and best practices in user experience research.
• Provide thought leadership and guidance on emerging UX trends and innovations.
• Keep up to date with the latest UX practices, innovations and tools

Lead CX/UX Research Consultant – AI-Enabled Experiences

• Lead computerized system validation (CSV) activities for regulated digital and AI applications throughout the SDLC
• Develop and execute validation deliverables including Validation Plans, Risk Assessments, IQ/OQ/PQ documentation (where applicable), test scripts, traceability matrices, and Validation Summary Reports
• Partner with Business Analysts, Quality Assurance, IT, vendors, and project teams to ensure systems meet business and regulatory requirements
• Review software requirements, functional specifications, design documentation, and change controls to ensure validation readiness
• Design, execute, and document risk-based testing strategies that demonstrate systems perform as intended
• Create and maintain validation evidence in accordance with internal procedures and regulatory expectations
• Support system implementations, upgrades, patches, and application enhancements
• Review and approve validation-related change controls and ensure ongoing compliance for validated systems
• Investigate test failures, identify root causes, and collaborate with technical teams to resolve issues
• Participate in internal audits, sponsor audits, and regulatory inspections by providing validation documentation and subject matter expertise
• Contribute to continuous improvement initiatives that enhance validation processes, testing efficiency, and compliance

Senior Validation Analyst, Clinical Research

• Ensures optimal quality of medical care for patients participating in study; uses ethical conduct as established for healthcare personnel.
• Assists in formation of educational aides and manuals as reference framework for patients and staff as necessary.
• Participate in continuing education programs.
• Educate nursing staff to drug protocols.
• Assist with updating policies/procedures.
• Keep abreast of new methods of treatment including the various venous access devices in the field.
• Arrange follow-up visits with patient to assess optimal quality of care and applies appropriate physical and psychological assessment to determine any effect of study drug.
• Implement appropriate intervention in the event of adverse patient response.
• Assess patient eligibility for inclusion in investigational studies.
• Review patient history and abstracts and records information; records pre-study lab data; secure baseline laboratory blood work from patient and arrange necessary scans.
• Review "informed consent" with patient; coordinate and educate patient and medical personnel as to required follow-up tests to be performed; assist physician in preparing IRB documents and maintain correspondence with sponsoring company/agency and IRB.
• Assure adherence to study requirements according to protocol; monitor study drug according to protocol; monitor and/or perform pharmacokinetic studies as detailed in protocol and attend to laboratory procedures to process, store and ship specimens.

Research Nurse Specialist

• Conducting research into international legal services markets through face-to-face and virtual interviews, by email and online
• Assessing research results to compile rankings of the top legal practitioners
• Presenting findings as succinct, engaging and accurate written copy
• Identifying trends and developments in the legal markets we cover
• Generating new research leads and content ideas for the reports
• Evolving our research methodology to produce as comprehensive and accurate reflections of the legal market as possible

Associate Research Analyst – Lexology Index

• Gain experience and insight into drug discovery and development
• Complete four 6-month job rotations in diverse R&D disciplines
• Work on meaningful assignments and projects
• Participate in mentorship, coaching, and collaborative interactions to develop business acumen and technical expertise

Research & Development Rotational Program Associate

• Support implementation and analysis of the client’s quantitative research projects
• Support the development of the questionnaires, polls, and other research instruments
• Support analysis of the data gathered via quantitative or multi-source data and research
• Program and deploy surveys and polls in Qualtrics
• Pull the target list for research deployment from various sources/systems
• Create cross-tabs and verbatim files
• Append data and customer information
• Assist in writing and editing reports and presentations for stakeholders
• Undertake curation of the Market Intelligence repository of research reports and related materials
• Lead tracking of the research projects across the enterprise
• Support expansion of the VoC and VoE programs, including future integration with Salesforce, API, etc.
• Additional responsibilities will include maintaining and over-time managing the clients' Customer Panel

Market Research Analyst

• Formulate in-depth investment recommendations based on fundamental analysis, valuation and risk assessment across the emerging immunology landscape
• Collect and rigorously analyze data related to therapeutics and various diseases, including scientific papers, clinical data, and KOL perspectives
• Design and execute primary market research, including market surveys and expert interviews, synthesizing findings into differentiated investment insights
• Build, maintain, and refine financial models, including DCFs, probability adjusted revenue forecasts, and scenario analyses
• Author research reports, initiation notes, and company updates for distribution to Leerink Partners’ institutional clients and sales force
• Engage directly with institutional clients and internal stakeholders to communicate investment views and respond to market-driven inquiries
• Monitor news, data releases, and regulatory updates across the coverage universe, providing timely commentary to clients and the sales force
• Support senior equity analysts at medical and industry conferences

Equity Research Associate – Emerging Immunology

• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
• Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.
• Gains an in-depth understanding of the study protocol and related procedures.
• Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
• Performs remote and on-site monitoring & oversight activities using various tools to ensure Data generated at site are complete, accurate and unbiased and subjects’ right, safety and well-being are protected.
• Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.
• Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.
• Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.
• Identifies, assesses and resolves site performance, quality or compliance problems and escalates per defined CRA Escalation Pathway as appropriate in collaboration with CRA-Manager, CRM, TA Head and CRD as needed.
• Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites.
• Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.
• Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor and sharing best practices as appropriate/required.
• Supports and/or leads audit/inspection activities as needed.
• Performs co-monitoring visits where appropriate.
• Following the country strategy defined by CRD and/or CRA-Manager, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities.

Clinical Research Associate, Oncology

• accountable for performance and compliance for assigned protocols and sites
• ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures
• acts as primary site contact and site manager throughout all phases of a clinical research study
• develops and expands the territory for clinical research, finding and developing new sites
• performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents
• conducts site visits and maintains clear, comprehensive and accurate visit & non-visit contact reports
• communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, regulatory documentation, site audits/inspections
• identifies, assesses and resolves site performance, quality or compliance problems

Clinical Research Associate – Immunology

• The role is accountable for performance and compliance for assigned protocols and sites in a country.
• Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally.
• Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.
• Actively develops and expands the territory for clinical research, finding and developing new sites.
• Performs remote and on-site monitoring & oversight activities to ensure:
• Data generated at site are complete, accurate and unbiased.
• Subjects’ right, safety and well-being are protected.
• Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits.
• Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.
• Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites.
• Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.
• Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor and sharing best practices as appropriate/required.

Clinical Research Associate, Cardiovascular, Vaccine, Infectious Disease

• Provide intellectual leadership for the Center's research and assessment initiatives.**
• Advance original scholarship, lead assessment development and validation efforts, and translate research into practical tools.**
• Oversee the ongoing development, validation, application, and commercialization support of proprietary assessment tools.**
• Conduct and publish original research related to entrepreneurship, innovation, leadership, and enterprise value creation.**
• Produce peer-reviewed publications, conference presentations, and practitioner-focused research.**
• Mentor undergraduate and graduate students participating in research projects.**
• Build relationships with researchers, institutions, and industry partners that advance the Center's research mission.

Associate Director of Research

• The Senior Research Analyst responds to complex legal, corporate, and industry research requests, meeting the daily information needs of firm lawyers, business professionals and clients using industry-standard databases and tools
• This role conducts research at an advanced level, evaluates sources, organizes findings into high-quality work product, manages workflow priorities and deadlines with sound judgment and accountability, and takes a proactive role in promoting Research Services tools, offerings, and services throughout the firm
• Lead research strategy for all sophisticated queries
• Exercise judgment and accountability in prioritizing billable workflow and either meeting or communicating effectively around deadlines
• Develop and maintain a keen understanding of the information needs, workflow, and preferences of users and stakeholders in order to support and improve ease of access to information

Senior Research Analyst

• Provides market research support in compiling and publishing high quality, comprehensive analysis
• Integrates the broader organizational and industry context into advice and solutions
• Solves complex problems requiring analysis of multiple variables
• Uses advanced methods to contribute to new solutions
• Develops and maintains contact with market participants
• Conducts meaningful analysis at the functional or enterprise level

Equity Research Associate – Enterprise Software

• Provides market research support in compiling and publishing high quality, comprehensive analysis and research on individual corporations, industries, financial markets, and economic developments as assigned.
• Expert level professional role requiring in-depth knowledge/expertise in own domain/field of specialty and working knowledge of broader related areas to run data analysis and develop research reports
• Solves complex problems requiring analysis of multiple variables, which may require consultation with multiple stakeholders
• Uses advanced methods to contribute to new solutions and recommend standards against which others will operate
• Interprets guidelines, standards, policies, and results of analysis to inform decision making at senior levels
• Builds stakeholder alignment in leading activities, identifying, and leading problem resolution

Equity Research Associate – Connectivity Semiconductors, Networking

• Manage programming and deployment of surveys and polls
• Assist with writing/editing reports and presentations of findings
• Collaborate on initiatives aimed at continuous VoC program improvements
• Support development and implementation of the new ASME customer panel

• As our first Research Associate, you will play a foundational role in building the operational infrastructure that makes Nourish's prospective clinical research possible.
• Own the systems, processes, and study execution from protocol design through data collection
• Design and execute IRB protocols for strategically important clinical studies
• Manage patient enrollment, draft white papers, conference abstracts, and contribute to peer-reviewed publications
• Work closely with clinical operations, product, data, and commercial partners

Research Analyst jobs in New York

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AVP, Research Analyst

Clinical Research Associate

Editor – Research Operations Analyst

Principal Associate, Market Research

Lead CX/UX Research Consultant – AI-Enabled Experiences

Senior Validation Analyst, Clinical Research

Research Nurse Specialist

Associate Research Analyst – Lexology Index

Research & Development Rotational Program Associate

Market Research Analyst

Equity Research Associate – Emerging Immunology

Clinical Research Associate, Oncology

Clinical Research Associate – Immunology

Clinical Research Associate, Cardiovascular, Vaccine, Infectious Disease

Associate Director of Research

Senior Research Analyst

Equity Research Associate – Enterprise Software

Equity Research Associate – Connectivity Semiconductors, Networking

Market Research Analyst

Research Associate