Research Analyst

• Leads, publishes, communicates, and contributes to research and analysis on industrial heat efficiency and electrification
• Develops thought leadership on industrial market transformation
• Works with the team to identify, monitor, and describe technology advances and policy windows to advance the market at the corporate, state, and federal levels
• Engages in outreach to states for industrial programs and rulemaking efforts
• Promotes, coordinates, and contributes to convenings and collaborations of utilities, industrial companies, NGOs and other partners to help advance energy efficiency and carbon reductions
• Develops and follows project workplans and meets milestones within budgeted hours
• Interacts with funders and develops new funding sources
• Contributes to proposal development.

Senior Research Associate, Industry Program

• Develop and execute client engagements based upon strategies co-created with senior executives.
• Support research and advocacy team, as well as collaborating with and supporting on communications and PR activities for clients.
• Manage regular client touchpoints and meetings by creating and updating agendas and client-facing materials, establishing clear next steps and ensuring follow-up notes are submitted to clients in a timely manner.
• Analyze publicly available data sets and create client-facing materials (e.g., decks, briefing documents)
• Approach work with a learning mindset and be open to giving and receiving candid feedback.
• Bring a critical eye to work and strive to develop and deliver final products that exceed expectations.
• Operate with wisdom, accuracy and speed in a fast-paced working environment.

Associate, Research and Advocacy

• 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 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

• Leading a Program Review team to consider changes to Defense Components' Program Objective Memoranda to ensure compliance with DOW guidance or to better align programs with the defense strategy.
• Conducting studies and assessing the efforts within the division portfolios: logistics and sustainment, intra-theater mobility, inter-theater mobility, irregular warfare, special operations, autonomous systems, counter-drone, and burden sharing programs.
• Analyses include assessments of technological and acquisition risk associated with developing and fielding capabilities.
• Generating and presenting the findings of analyses to senior leaders and nontechnical audiences, clearly and concisely.
• Ensuring analytic techniques used are valid and appropriate to the problem or issue identified.

Operations Research Analyst – Global Shaping Division

• Serve as study manager for FDA, NIH and industry-sponsored and investigator-initiated research studies by implementing reliable methods to support clinical research activities.
• Contribute scientific, clinical, data, and technical expertise to guide the execution of complex research projects.
• Leading research focus interactions with clients in the medical device and pharmaceutical industries and provide clinical registry expertise and guidance to support custom data analytics and research study requests.
• Reviewing inbound research questions, requests, and study protocols to determine the feasibility of conducting studies within the context of the NCDR infrastructure.
• Working closely with physician members, and member committees to facilitate clinical, scientific, and strategic review of new research proposals.
• Work closely with the data analytics team and data analytics centers to review and assess the suitability of research proposals.
• Work closely with the data analytics team and data analytics centers to facilitate the completion of accepted projects.
• Drafting study procurement documents that accurately capture the scope of work to be performed and translate client requests into statements of work, project budgets, and project contracts.
• Coordinating the activities of internal and external cross-functional teams and monitor the progress of study milestones and deliverables, ensuring quality and timeliness of project deliverables.
• Preparing and submitting IRB applications.
• Ensuring alignment of budgets with study needs and responsible for invoicing and tracking revenue and expenses for the life of the study.
• Preparing and submit project status and effort reporting to stakeholders, including federal agencies, industry, committees, and internal staff.
• Represent ACC on internal and external groups, as assigned. Build and maintain excellent relationships with internal and external partners and clients.
• Anticipate risk and identify challenges early on and communicate project risk as well as possible risk solutions to Team Lead.
• Work with internal IT teams, NCDR registry product managers and others as appropriate to ensure the logic and application of registry data for various study types. Serve as a liaison between ACC registry management teams and external research partners.

Associate, NCDR Research Studies

• 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

• Ensure the capture of program data.
• Produce reports based on program data.
• Monitor the commitment and obligation of funds.
• Prepare reports on disbursement of funded research or demonstration projects.
• Help translate scientific evidence from the literature into practical information.
• Support ongoing coordination and management of program activity.

Research Analyst – Non-Data

• Clean, structure, code, and summarize survey and secondary data
• Use statistical software (SPSS, R, etc.) and business software (Excel) to uncover and evaluate solutions, and assist project staff in running statistical analyses
• Apply programming skills (Excel VBA, Python, etc.) to help automate standard statistical procedures and chart creation.
• Demonstrate your understanding of multivariate analysis and Ipsos proprietary products, and work with Client Service from understanding business questions to design, analysis, and application
• Work from an analytic plan, assemble Excel outputs or PowerPoint decks to provide results and explanations for Client Service
• Consistently ensure the timely delivery of error free work

Research Analyst, Global Modeling Unit

• Manage the Hoya Harvest Garden
• Provide food to those in need
• Educate about sustainable agriculture
• Engage with faculty and fellows from across the university
• Support multidisciplinary faculty in completion of their work

Research Associate

• Produce UPO’s District of Columbia Triennial Community Needs Assessment
• Develop and implement a 12-month data gathering and assessment plan to complete a comprehensive, city-wide needs assessment survey including, but not limited to, analysis of quantitative (surveys) and qualitative data (focus groups/targeted interviews), literature reviews, community asset mapping, and case studies, etc.
• Author the needs assessment adhering to prevailing standards of writing, citation, and ethical use of sources.
• Coordinate with the Director of Business Development and Asset Management to execute a workplan to complete the needs assessment.
• Coordinate with UPO inter-office staff to analyze qualitative and quantitative data and other information.
• Prepare presentations for reporting to UPO leadership, board members, and general public relative to findings of the needs assessment.
• Recommend priority areas for strategic program development responsive to the needs assessment.
• Support UPO staff, volunteers, and interns engaged in the needs assessment process.
• Routinely collect, analyze, and present relevant information and data that inform strategic decisions.
• Perform analyses on US Census data relevant to low-income communities.
• Support business development efforts by conducting thorough research requested by executive leadership that influence strategic decision making.
• Support the organization’s grant development function by drafting research and developing content needed for grant proposals, when needed.
• Support post-award reporting of grant-funded programs, when needed.
• Provide the office with administrative support including obtaining financial and grants management reports, tracking rental data, and liaising on special projects.
• Work with third-party consultants to gather information to inform special reports and studies.

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