Research Analyst

• Maintain consistent review of accounts receivable. This includes:
• Review charges daily that are in the Epic charge review workqueues and Epic reports to segregate them as research paid, routine care, or not study related.
• Ensure technical and professional charges are segregated based on each study’s billing grid.
• Apply appropriate billing modifiers and other requirements for billing research-related charges to federal and non-federal payors.
• Processes charge related corrections, additions, and removals in Epic and the OnCore CTMS to ensure organizational compliance.
• Refer to study documents (e.g. study protocol, informed consent form, Clinical Trial Agreement (CTA), billing grid) when reviewing research patient accounts to ensure maximum revenue from study fees through timely and accurate billing.
• Communicate with study teams, revenue cycle teams, and others to resolve billing related issues.
• Generates invoices in the OnCore CTMS based on the study’s Billing Grid and contract.
• Track invoices from third-party vendors to ensure correct billing of research-related procedures. Collaborate with finance team to ensure vendors receive timely payment for services.
• Collaborate with the PI/study team, Office of Research staff, and other Inova departments to determine accurate Current Procedural Terminology (CPT) coding for billable procedures. Serves as a resource to communicate with non-research departments to determine correct coding and charges.
• Collaborates with the study teams and Office of Research personnel in the development and implementation of educational activities related to research billing compliance.
• May assist other personnel in month end close of research accounts.

Clinical Research Revenue Integrity 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

• Provide content and technical support to survey respondents via e-mail and phone.
• Assist with survey documentation including data collection procedures.
• Participate in detailed reviews of survey data.
• Assist with reports and analyses as directed.
• Software and survey testing.
• Qualitative tasks such as focus group and interview note taking, recruitment, and arranging logistics.
• Some data entry and other administrative tasks (e.g., note taking).

• Conduct research that informs policy, strategy, and decision-making on issues of interest to the quantum industry.
• Contribute substantively to the conception, development, and dissemination of research and policy analysis.
• Support a portfolio of projects by conducting rigorous inquiry, produce high-quality and persuasive written analyses, engage with stakeholders, and assist in the development and stewardship of externally funded research awards.
• Lead the production of a wide range of research products, including policy briefs, technical reports, white papers, and presentations.

Policy Research Associate

• Act as the primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.
• 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 International Conference on Harmonization / Good Clinical Practices, 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 and manages various tasks in collaboration with other sponsor roles to achieve Site Ready
• Participates and provides inputs on site selection and validation activities
• Performs remote and on-site monitoring & oversight activities using various tools 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, closeout 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 Clinical Research Manager and Partner Line Manager
• Manages and maintains information and documentation in Clinical Trial Management System, electronic Trial Master File and various other systems as appropriate and per timelines
• Contributes to CRA team knowledge by acting as process Subject Matter Expert, buddy/mentor and sharing best practices as appropriate/required
• Supports and/or leads audits/inspection activities as needed
• Performs co-monitoring visits where appropriate

Clinical Research Associate – Oncology

• Support Army logistics materiel management programs through supply management, inventory analysis, warehousing, and strategic initiatives.
• Conduct research and analysis to evaluate materiel management operations, inventory performance, supply chain effectiveness, and emerging issues.
• Collect, consolidate, validate, and analyze information from multiple data sources to support executive decision making and program recommendations.
• Develop executive-ready briefings, reports, decision papers, presentations, and other written communications supporting Army logistics materiel management initiatives.
• Support planning, coordination, and continuous improvement of warehousing, secondary item management, inventory control, and supply management processes.
• Coordinate activities and recommendations across multiple Army organizations and stakeholders to support enterprise materiel management objectives.
• Monitor project activities, milestones, deliverables, inventory trends, and action items to ensure timely execution.
• Facilitate meetings, working groups, and collaborative planning sessions while documenting decisions and tracking follow-up actions.
• Synthesize complex operational and analytical information into actionable recommendations that improve supply chain performance, materiel readiness, and organizational effectiveness.
• Develop performance metrics, dashboards, and analytical products to support leadership visibility and informed decision making.
• Support strategic planning, inventory assessments, supply chain analysis, and enterprise modernization initiatives, as required.
• Support business development activities, including market research, proposal support, solution development, and client engagement, as required.
• Perform additional consulting, analytical, and project support activities as assigned.

Operations Research Analyst – Mortuary Affairs

• Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance.
• Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials.
• Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience.
• Considered as the primary point of contact for the investigative site.
• High level of competency or experience in providing contextual information on the clinical trials, connects stakeholder to the investigative sites and strengthens AbbVie’s positioning.
• Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program, protocol and patient treatment principles for the trial ensuring a trusted partnership.
• Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards, ensuring safety and protection of study subjects.
• Advanced understanding of site engagement and ability to customize site engagement strategy for assigned study (ies).
• Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy.
• Advanced level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities.
• Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey.
• Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance.
• Possesses experienced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development.
• May participate in global/local task forces and initiatives.
• Responsible for activities as assigned by manager.
• Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues.
• Advanced ability to think critically to resolve site risk signals while having robust understanding of site processes to drive study execution.
• Ensures preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance using a customer centric approach.
• Identifies, evaluates and recommends new/potential investigators/sites on an on going basis.
• Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
• Ensures audit and regulatory inspection readiness at assigned clinical site at all times.
• Manages investigator payments as per executed contract obligations, as applicable.

Clinical Research Associate II

• 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

• Work with Clearinghouse stakeholders to expand usage of Clearinghouse data
• Contribute to research on student enrollment, movement, and outcomes
• Collaborate with the Research Center team using Clearinghouse data for quantitative research
• Support development of data reports and publications
• Assist in requirements gathering and client relationship management
• Manage multiple research projects/assignments simultaneously
• Perform quality control checks to ensure accuracy and timeliness
• Build trust with stakeholders by demonstrating consistency between words and actions

Research Analyst – Research Development, Philanthropy

• Develop, maintain, and analyze Integrated Master Schedules (IMS) for large, complex DoD acquisition programs.
• Perform schedule risk assessments for weapon system programs, including the development of schedule logic, identification of driving paths, and critical dependencies.
• Conduct Schedule Risk Analysis (SRA) using Monte Carlo simulation techniques to quantify schedule uncertainty and identify key risk drivers.
• Provide actionable recommendations to mitigate schedule risks and improve program execution.
• Support planning and execution of customer engagements, including standing up new schedule management processes or improving existing processes.
• Interface directly with government program managers, technical leads, and executive leadership, delivering clear, concise schedule briefings and decision-support products.
• Support proposal efforts, contract start-up activities, and transition-in planning as required.

Operations Research Analyst, Associate Principal

• Support the Office of Critical Technologies in modern research and analysis of strategic biotechnology initiatives.
• Advise Pentagon leadership on biotechnology issues.
• Evaluate and secure technology for national defense modernization.
• Represent on Integrated Product Teams (IPTs) and participate in government conferences.
• Conduct biotechnology research analysis and prepare presentations to DoD leadership.

Research Associate, Associate Principal

• Collaborate with team members to ensure all project deadlines are met and project logistics are accounted for
• Assist in all aspects of research across operational phases throughout the project, including survey proofing, data cleaning, data charting, data checking, recruitment updates, etc.
• Document client calls and internal meetings, including providing feedback to the relevant projects and ensuring documentation is shared with team for collaboration
• Support client deliverables by creating slides, identifying case studies, syndicated data and desk research that lend to the overall insights and narrative
• Manage logistical issues around fielding, data processing, vendors, etc., including identifying process improvements
• Proactively communicate availability/capacity/contributions to the team

Research Analyst – Custom Market Research

• Support the DoD Executive Agent for Anti-Tamper with policy development, exportability guidance and enterprise-wide AT planning in support of exportability
• Advise senior DoD leaders and the DoD AT Enterprise (consisting of the EA and the services) on how to optimally integrate policy with processes driven by Exportability Reform, Acquisition Transformation and Tech Release/Force Disclosure Reform
• Advise senior DoD leaders and the DoD AT Enterprise (consisting of the EA and the services) on how to optimally implement exportability strategies as a result of:
• New & updated Executive Orders
• New & updated Office of Secretary of War (OSW) (Research & Engineering) Program Protection & CPI guidance and policies (DODI 5000.83)
• New & updated OSW (Acquisition & Sustainment) acquisition processes with Defense Exportability Features (DODI 5000.85)
• Advise senior DoD leaders and the DoD AT Enterprise (consisting of the EA and the services) on CPI requirements, program protection strategies, AT modernization, and compliance with DoD policy
• Assist with CPI evaluations for non-program-of-record programs
• Support the performance of horizontal protection analyses to identify vulnerabilities and cross-program protection gaps for exportability in accordance with DoDI 5230.28
• Author program protection documentation, risk assessments, white papers, technical reports, acquisition documentation, and leadership briefings and decision-support materials tailored for senior leadership and the ATEA
• Advise on the identification, classification, and protection of Critical Program Information across RDT&E programs in accordance with DoDI 5200.39 and DoD policy
• Advise on and optimize how the DoD ATEA, specifically as directed under the DoDD 5200.47E, integrates with these processes

Anti-Tamper / Critical Program Information SME – Operations Research Analyst 4

• Collect, analyze, and interpret data to generate actionable insights that inform the Total Rewards COE strategies and initiatives.
• Develop measurement frameworks to assess the impact of learning programs, leadership development initiatives, talent acquisition, performance & succession management programs, and key talent interventions.
• Conduct ROI studies and effectiveness evaluations for Total Rewards COE initiatives.
• Conduct comprehensive pay equity analysis across different demographics, present findings and develop the strategy to address any identified disparities.
• Ensure accuracy and integrity of data by maintaining standards and governance practices.
• Assist in the design, implementation, and maintenance of COE tools, templates, and methodologies.
• Utilize total rewards data (ex. compensation, benefits usage, promotion cycles) in conjunction with other PP data (ex. tenure, performance reviews) to identify at-risk employee segments and propose targeted retention strategies.
• Drive innovation by moving from standard reporting to building predictive models that forecast compensation and benefits trends.
• Collaborate with PP Business Partners, functional leaders, and key stakeholders to understand needs and areas for innovation.
• Respond to inquiries and provide guidance on COE processes, tools, and systems.
• Support change management and communication efforts related to COE projects.
• Partner with the Health & Welfare Solution Specialist to evaluate the return on investment (ROI) of existing benefits programs by analyzing participation rates, cost per hire, and employee satisfaction data.
• Partner with the Compensation & Retirement Solution Specialist to improve salary and bonus modeling processes to increase efficiency and accuracy in advanced comp cycles.
• Recommend process improvements and innovative solutions to enhance efficiency, support a best-in-class employee experience and drive adoption.
• Contribute to knowledge management by documenting and sharing COE resources and learnings.

Total Rewards COE Research Analyst

• Conducting thorough research into an individuals’ background using a variety of tools, such as databases and public records
• Gathering information, analyzing data, and compiling this information to be entered into a final report
• Processing searches related to background screening reports
• Ensuring all searches are processed and reported according to state and federal laws as outlined in AccuSourceHR’s reporting guidelines
• Ensuring all searches are processed according to client guidelines
• Retrieving public records information and entering said information into our platform
• Analyzing information and comparing data sets to confirm matching identifiers
• Performing other duties as assigned
• Meeting or exceeding minimum standard service requirements

Research Specialist

• Utilizes expertise in machine learning and advanced statistical methods to analyze data sources
• Provides guidance to teams in optimal use of Artificial Intelligence in data analytics
• Oversees and mentors other analysts as directed by the Director
• Leads data risk assessments and identifies data quality and security issues
• Provides consultation regarding statistical methods and analysis designs
• Conducts predictive and geospatial data analytics
• Serves as HAI representative to the DoHS for project planning and performance
• Prepares reports required by the University and external agencies

Research Associate Analyst – Health Affairs Institute

• Support the development of written, web-based, and training and technical assistance products, including briefs, reports, tools, and presentations
• Conduct background research and synthesize findings through literature reviews, systematic evidence reviews, evaluation reports, and practitioner- and policy-oriented briefs
• Provide foundational quantitative research and evaluation support, including programming in statistical software and conducting basic statistical analyses
• Assist with qualitative research activities such as instrument development, coding, synthesis, and documentation
• Develop and maintain workflow protocols, templates, and project tracking tools to support high-quality, on-time deliverables
• Contribute to internal knowledge management and support team collaboration across projects

Research Analyst – On-Call

• Serves as a University representative and liaison to the West Virginia Department of Human Services
• Work as part of a team to advance the partnership between the West Virginia University Health Sciences Center and the West Virginia Department of Human Services
• Facilitates communication and efficient collaboration between research partners
• Oversee and conduct analyses of Medicaid claims data using SAS and other statistical analysis packages
• Support West Virginia University faculty and leadership within the Department for Human Services
• Train other West Virginia University faculty in analyzing Medicaid claims data
• Ensure compliance with university-level policies for responsible conduct of research
• Provide consultation to faculty and government partners regarding preparation of research proposals
• Identify opportunities for potential collaborations
• Prepares reports as required by the University
• Communicates results of analytic projects and program evaluations with relevant staff
• Conducts or directs special projects as assigned
• Assist with the publication of peer-reviewed manuscripts

Research Analyst jobs in Virginia

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