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

• Conduct hyper-targeted lead generation focused on commercial property managers, facilities directors, building owners, and decision-makers
• Source and identify 20-30 qualified prospects per day
• Research commercial properties and gather relevant building information
• Cross-reference business addresses and verify accuracy
• Identify, verify, and update contact information
• Maintain a clean and accurate CRM database
• Draft personalized outreach emails
• Support business development efforts
• Assist with backend operational workflows and administrative tasks
• Provide clear end-of-day updates

Lead Generation & Research Specialist – B2B Prospecting Support

• Provide project management and logistical support for multiple research hubs and studies
• Support operations of complex research projects and assist in data management
• Build relationships with external collaborators and team members
• Maintain meeting agendas and follow up on action items
• Participate in research activities including developing protocols and conducting interviews
• Support project-related communication and deliverables
• Organize and execute project events and track project milestones

Research Associate

• Work collaboratively with internal Process Development and Analytical Development teams.
• Assist with experimental execution in support of molecular assay development and qualification, including ddPCR/qPCR-based methods.
• Perform routine molecular analytics (e.g., ddPCR) and provide data in a timely manner to support process studies.
• Support development and execution of lentiviral vector characterization assays for process development and process characterization activities.
• Author ELNs, methods, reports and SOPs.

Senior Research Associate – Analytical Development

• 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

• Execute molecular and cell biology protocols, including flow cytometry, quantitative PCR, western blots, RNAseq and associated data quantification/analysis
• Assist with imaging experiments, including confocal and mass spec imaging and associated data quantification/analysis
• Human and mouse cell cultures
• Contribute to the development of new protocols as needed
• Present results and summarize progress to help frame internal decision-making
• Comply with SOPs, good laboratory practices, and regulatory requirements
• Adhere to a team schedule and individual time management
• Maintain accurate laboratory documentation using established methods
• Train new lab members in molecular, cellular, and imaging techniques
• Other duties as assigned

Research Associate III – Integrative Metabolic Biology

• As a Market Research Analyst, you will own the end-to-end execution of quantitative research projects, supporting stakeholders through the full research lifecycle—from survey design and programming to data analysis, reporting, and insight development.
• You will manage multiple projects simultaneously, ensuring high-quality deliverables, accurate data processing, and timely communication of project progress.
• This role requires strong expertise in survey methodology, survey programming, data analysis, and reporting, along with exceptional attention to detail and the ability to translate complex findings into clear, actionable business insights.

Market Research Analyst

• 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

• 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

• Perform on-site and remote monitoring visits to ensure subject safety and data quality
• Review CRFs and source documentation for accuracy and completeness
• Ensure informed consent procedures and protocol compliance are met
• Manage and track Investigational Product accountability
• Prepare monitoring visit reports and follow up on action items
• Maintain and update eTMF, CTMS, and trial documentation systems
• Support sites with issue resolution and ensure timely completion of deliverables
• Participate in audits and inspections, including preparation and follow-up
• Collaborate with project teams and contribute to monitoring plans, project tracking, and CRA resource planning

Senior Clinical Research Associate

• Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients
• 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, provides 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 under supervision 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 under supervision, in compliance to the protocol and monitoring plans and accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and to quality standards in conducting clinical research, ensuring safety and protection of study subjects
• Customize site engagement strategy for assigned study (ies) under supervision
• 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
• Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey
• 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
• Ensures preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance

Clinical Research Associate I – Oncology

• Collect fish and environmental data in freshwater, estuarine, and nearshore marine environments of the West Coast region.
• Conduct field work outdoors in or around water, including in sometimes harsh conditions.
• Drive vehicles and/or boats and trailers, and provide occasional assistance on ship surveys lasting days to weeks, as needed.
• Implement occasional laboratory experiments and data processing activities.
• Conduct data visualization and analysis.
• Conduct literature reviews to extract data and published relationships between ecological outcomes and potential stressors or habitat metrics.
• Collaborate with team members to produce tools that improve transparency and efficiency of management decision making and permitting.
• Share comprehensive workflow protocols and research products so others can easily interact with them and understand what was done.
• Write reports, contribute to journal manuscripts, and present results at regional meetings and scientific conferences, as needed.
• Participate reliably in field and/or laboratory activities coordinated by the NWFSC.
• Document that samples or data were collected, stored, and processed using established protocols.
• Maintain reproducible workflows and store analysis products in an accessible and organized way.
• Provide written status reports and other ad hoc communications, as needed.

Fisheries Research Associate – Field, Lab, Data Support

• 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

• Performing legal and policy research and analysis.
• Drafting bills, amendments, and other legislative documents.
• Developing and evaluating policy alternatives to assist Senators in meeting their goals.
• Presenting legislation and other policy matters before committees.
• Monitoring and analyzing implementation efforts by state and local government agencies.
• Responding to inquiries on pertinent policy issues.
• Developing appropriate professional relationships with Senators, other legislative staff, state agency staff, and interest groups.

Staff Counsel/Research Analyst

• perform experiments using in vivo electrophysiology, carefully controlled mouse behavior, and neural manipulations
• collaborate with scientists to develop and evaluate new behavioral tasks and associated methods for data collection, quantification, and analysis
• collaborate internally and externally to analyze physiology and behavior data
• participate in weekly lab meetings
• train team members to perform procedures

Research Associate II, In Vivo Electrophysiology, Behavior

• Develop SAS programs for validating surveillance, clinical, or research study data.
• Verify that all variables that should be included in the resulting dataset are present in the dataset and extraneous variables are excluded.
• Identify data discrepancies and other inconsistencies in the resulting dataset.
• Develop codebooks and data management plans.
• Run duplicate procedures and comparison of results to ensure validity with applicable standards of the resulting final data sets, indicators, questionnaire coding, metadata set, SAS programming, and output files.
• Conduct geospatial and molecular HIV analysis and interpret results using R.
• Work collaboratively with other analysts to develop novel code in support of analyses.
• Support dissemination and reporting of data to internal and external partners.
• Work alongside federal partners to support funded jurisdictions or funded CBOs.

Research Analyst, SAS, R

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
• Conduct study initiation visits (SIVs)
• Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements

Senior Clinical Research Associate – CNS/Psychiatry

• 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 jobs in Washington

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