Research Analyst

• Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study
• Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conduct the clinical study throughout the study period
• Trains investigational site staff as necessary
• When applicable, supports preparation of regulatory and / or EC submissions
• Participates in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance.

Senior Clinical Research Associate

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.
• Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans.
• Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes.
• Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate.
• Demonstrates diligence in protecting the confidentiality of each subject/patient.
• Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
• Assesses site processes according to the Clinical Monitoring/Site Management Plan (CMP/SMP).
• Conducts Source Document Review of appropriate site source documents and medical records.
• Verifies required clinical data entered in the case report form (CRF) is accurate and complete.
• Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines.
• Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture.
• Verifies site compliance with electronic data capture requirements.
• May perform investigational product (IP) inventory, reconciliation and reviews storage and security.
• Verifies the IP has been dispensed and administered to subjects/patients according to the protocol.
• Verifies issues or risks associated with blinded or randomized information related to IP.
• Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned.
• Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness.
• Reconciles contents of the ISF with the Trial Master File (TMF).
• Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations.
• Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.
• Supports subject/patient recruitment, retention and awareness strategies.
• Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution.
• For assigned activities, understands project scope, budgets, and timelines; manages site-level activities/communication to ensure project objectives, deliverables and timelines are met.
• Must be able to quickly adapt to changing priorities to achieve goals/targets.
• May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate.
• Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements.
• Prepares for and attends Investigator Meetings and/or sponsor face to face meetings.
• Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements.
• Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.

Experienced Clinical Research Associate – Sponsor Dedicated

• Track proposed legislation, regulations, and public policy developments relevant to the firm's practice areas and client base; synthesize findings into timely, actionable intelligence.
• Research, draft, and produce in-depth reports, issue summaries, comparative analyses, and timelines on proposed laws and regulatory actions — proactively delivering intelligence before it is requested where possible.
• Leverage AI platforms and research tools to design and build systems for legislative monitoring, alerting, and stakeholder reporting; identify opportunities to expand and improve these systems over time.
• Provide research support across all practice groups and business units, responding to incoming requests with accuracy, thoroughness, and clear communication.
• Participate in the assessment and trialing of new research platforms and AI solutions; contribute to resource evaluations and provide informed recommendations.
• Collaborate effectively with peers to manage research requests received from attorneys, consultants and firm staff, contribute to department projects, and support the team's broader strategic goals.
• Assist with other research tasks and projects as required.

Research Specialist – Legislation Specialty

• Assists in the preparation and submission of regulatory documents to the study sponsor and IRB, as required by the protocol and regulatory requirements.
• Assist in the conduct and documentation of study visits and protocol-specific testing/interviews according to the study protocol.
• Assists the research team in completing case report forms accurately and according to the protocol.

Cancer Clinical Research Specialist 1

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborating with investigators and site staff to facilitate smooth study conduct
• Performing data review and resolution of queries to maintain high-quality clinical data
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Clinical Research Associate II

• Lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
• Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
• Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

• Responsible for fulfilling customer research requests for statements, check images, documents, etc.
• Support yearly processes for escheatment, expired W8s, processing W9 forms, and assessing tax reporting exceptions.
• Assist internal customers with inquiries and guide them through the applicable procedures.
• Complete outgoing wires for various processes.
• Legal order daily processing, such as levies, garnishments, freezes, legal document review, subpoenas.
• Work closely with other internal departments, branch staff, or the Call Center to complete all requests correctly.
• Complete all work within the established service level assignment to ensure timely input of changes, corrections and review of items originally processed by the branches daily.
• Deliver new hire, product, procedure, and system training to team members.

Deposit Ops Research Specialist

• Perform site management activities to ensure compliance with the protocol, monitoring plan, ICH GCP, local regulatory requirements, and client SOPs
• Conduct site qualification, initiation, interim, and close-out visits, both on-site and remotely
• Partner with Clinical Trial Liaison (CTL) and other client functions (e.g., Study Start-Up, Global Partnerships and Trial Optimization) to support site activation and deliverables
• Establish and maintain productive professional relationships with investigator site staff, ensuring effective communication and problem-solving throughout study conduct
• Perform drug accountability, reconciliation, and destruction, ensuring protocol compliance for storage and shipment requirements
• Prepare and maintain Oversight Monitoring Plan
• Perform review of study metrics, assess CRO Clinical Research Associate (CRA) and Investigator Site performance and identify sites for oversight monitoring visits
• Conduct Oversight Monitoring Visits at sites, either independently or alongside CRO CRA
• Review site source documentation and verify accurate data capture (ALCOA principles)
• Review and report on status of study conduct at the investigator site ensuring appropriate follow up of any identified issues/action items
• Ensure site regulatory files are current and verify timely submission of study documentation, including safety reporting
• Write and submit accurate monitoring visit reports, oversight monitoring visit reports, and study correspondence in a timely manner
• Periodically verify completeness of site documentation (e.g., investigator site file/regulatory binder contents)
• Identify and record protocol deviations, escalate non-compliance, and resolve study-related issues as necessary
• Track, trend, and report issues, escalating them to the appropriate teams when required
• Maintain ongoing communication with site personnel, study teams, CTLs, Central Monitors, and CRO CRAs
• Actively participate in team meetings and process improvement initiatives to enhance study outcomes
• Support inspection readiness activities and ensure sites maintain data integrity and protocol deliverables

Senior Clinical Research Associate – Oncology

• Investigate and research new home developments using Zonda’s proprietary research methodologies and tools
• Analyze and interpret data from multiple sources, even when information is limited or incomplete
• Keep project and community data accurate and up to date through online research, builder website reviews, public records, and satellite imagery analysis
• Identify trends, inconsistencies, and missing information with a sharp analytical eye
• Meet quarterly research deadlines with a strong focus on data integrity, consistency, and completion rates
• Share weekly insights and analytics related to data collection progress with leadership and the Research team
• Collaborate with a dynamic team while also owning your region and working independently with confidence

Research Analyst – Construction

• You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Clinical Research Associate

• Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study
• Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conduct the clinical study throughout the study period
• Trains investigational site staff as necessary
• When applicable, supports preparation of regulatory and / or EC submissions
• Participates in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance

• Conducts research and data analysis to develop insights and inform the public's understanding of financial capability and financial fraud prevention, using different statistical techniques and data from various sources.
• Produces research-based communications and publications, including reports, issue briefs, journal articles, visualizations, infographics, and presentations suitable for internal and external audiences.
• Manages research project coordination and stakeholder communication, ensuring timely completion and keeping internal and external partners informed of progress across multiple projects.
• Supports research dissemination and communications, partnering with corporate communications to promote research through briefs, via social media assets, website updates, press releases, and media outreach.
• Provides support to organizational leadership and internal stakeholders, including preparation of Foundation board materials and board metrics, as well as research and analysis support to other FINRA departments.
• Ensures research quality and integrity through quality control of analyses and statistics, including reviewing and validating statistical code and methodology.
• Supports research administration and governance, including the initiation and execution of legal agreements for research projects and participation in the FINRA Foundation's grantmaking activities.
• Demonstrates FINRA’s values.
• Collaborates with internal and external partners, both in-person and virtually, to advance FINRA's mission and the FINRA Foundation's mission.

Associate Principal Research Analyst

• Join an innovative and dynamic environment supporting the Office of the Corporate Chief Underwriter (OCCU)
• Dive into a variety of exciting projects and research initiatives
• Support protective value (PV) studies; creating RFPs for different vendors and vendor evaluation
• Examine and identify new data sources for research and insights
• Improve workflows and work on ways to increase automation
• Provide input on predictive modeling
• Revise underwriting rules and procedures
• Partner with leadership across the enterprise to champion changes that improve processes, while maintaining mortality expectations
• Shape data sources for data driven underwriting practices
• Provide recommendations around new technologies and methodologies for risk selection
• Analyze, create, and develop rules for algorithmic and accelerated underwriting processes
• Develop new and competitive underwriting guidelines with research, documentation, marketing, and presentations

Life Underwriting Research Consultant

• Performing selection, initiation, interim monitoring and closeout visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Clinical Monitoring Plan (CMP)
• Driving performance at the sites
• Proactively identifying and ensuring timely resolution to study-related issues and escalate them as appropriate
• Training, supporting and advising Investigators and site staff in study related matters, including Risk Based Quality Management (RBQM) principles
• Development of recruitment plans with each site and managing and supporting enrollment to ensure sites and studies meet enrollment milestones
• Document recruitment barriers and mitigation plans
• Preparing and finalizing monitoring visit reports in CTMS and provide timely feed-back to the Principal Investigator, including follow-up letter, within required timelines and in line with Alexion SOPs
• Ensuring timely collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, Alexion SOPs and local requirements

Senior Clinical Research Associate – East Coast

• Create the design and optimization of text analytics models in Qualtrics Engage / XM Discover, with a focus on rule-based topic modeling, taxonomy development, sentiment, effort, emotion, and tagging standards.
• Build scalable frameworks across multiple business units, ensuring consistency, clarity, and alignment within a complex and growing VoC landscape.
• Develop and maintain taxonomy and governance, including naming conventions, rulesets, documentation, and quality controls that keep our programs aligned across teams.
• Ensure the accuracy and integrity of classification by regularly performing model audits and ongoing maintenance to improve model capture and precision rates.
• Collaborate with other members of the CX team to make sure models reflect the real experience of our customers and support key measures like NPS, CSAT, CES, Exit Survey responses, and at-risk behavior indicators.
• Partner with business stakeholders to understand their needs, gather domain knowledge, and ensure text analytics structures appropriately support product, service, and experience priorities.
• Own project timelines and execution for text analytics development across different business units, ensuring timely updates and alignment with rollout plans.
• Support the broader CX team on select research projects such as journey mapping, qualitative interviews, or deep-dive analysis.
• Create and maintain clear documentation that enables others to understand the structure, purpose, and application of models and taxonomies.

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Senior Clinical Research Associate

Experienced Clinical Research Associate – Sponsor Dedicated

Research Specialist – Legislation Specialty

Cancer Clinical Research Specialist 1

Clinical Research Associate II

Senior Clinical Research Associate

Deposit Ops Research Specialist

Senior Clinical Research Associate – Oncology

Research Analyst – Construction

Clinical Research Associate

Senior Clinical Research Associate

Associate Principal Research Analyst

Life Underwriting Research Consultant

Senior Clinical Research Associate – East Coast

Customer Experience Research Analyst