Research Analyst

• 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

• 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

• Assist in the origination, underwriting, and monitoring of privately placed debt securities for institutional clients
• Perform in-depth due diligence including credit analysis, research, and financial modeling
• Prepare detailed investment memos and present recommendations for new investments
• Active management and surveillance of existing portfolio credits
• Engage with sell-side agents, sponsors and investment banks to build relationships
• Partner with various sales teams to drive broader business development

Senior Research Analyst

• 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

• 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
• Perform various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets
• Train sites to collect data properly and report any potential safety-related events
• Manage the site's activities during study maintenance and closing down research activities at the sites once the study has concluded

Senior Clinical Research Associate – CNS/Rare Disease

• Lead interviews with portfolio management teams
• Gather and analyze information to identify asset managers
• Provide insights and advice on equity investment strategies
• Present Mercer’s views at conferences
• Mentor and support the equity research team

Equity Research Specialist

• Coordinate and conduct all work in strict compliance with applicable safety requirements, containment requirements, standard operating practices, and/or guidelines.
• Assist in the design, build, screen/test, and cultivation of model and non-model organisms including bacteria, yeast, and fungi.
• Perform routine strain engineering workflows and general molecular biology procedures, including DNA and RNA isolation and purification, PCR, sequencing, ligation, assembly, chemical and electrical transformations, and conjugation.
• Development of high-throughput assays, including the design and implementation of plate-based growth assays using Agilent BioTek instruments.
• Perform batch fermentations in either microtiter plates or flasks and prepare samples for submission for downstream organic extraction.
• Support team members by preparing specific solid and liquid media, buffers and reagents to support synthetic biology workflows.
• Assist with QC and data collection as requested.
• Accurate and well-organized record keeping of all experimental work for the development of SOPs and maintenance of an electronic laboratory notebook.
• Prepare comprehensive slide presentations summarizing key points and results, effectively communicate findings to a larger audience as needed.
• Maintenance of the laboratory including general housekeeping functions, inventory maintenance and organization, and equipment upkeep.
• Assist in the onboarding of research technicians by overseeing training of general lab operations and molecular biology procedures, organizing a clear training schedule and coordinating with other lab members as needed.

Research Associate

• 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

• Investigate and interpret data, turning research into clear, concise executive memos, diagrams, and presentations.
• Support research for projects regarding business competitors and non-profit organizations.
• Collaborate with business units to understand their challenges and recommend solutions to senior management.
• Edit and proofread memos, emails, presentations and reports.

• Function as an internal consultant and program manager in marketing, strategy, product development, customer loyalty, internal operations, and business development initiatives
• Work with leadership, project staff, and inter-departmental staff/management teams to define objectives and identify key issues for each assignment
• Oversee project work of other team members
• Synthesize results into actionable insights, implications, and management recommendations
• Involved in the implementation of new initiatives

Senior Market Research Consultant

• Manage survey research projects, within timeline and budgets, including working closely with colleagues in our Operations groups to oversee all operational components of projects
• Design questionnaires and plan analyses
• Perform quality checks at various stages of the research to ensure accuracy, and to avoid errors or mistakes
• Manage the overall project timelines, ensuring that milestones are met and signed off at the various stages of the project execution
• Analyze and interpret survey results; prepare reports and presentations
• Develop an understanding of our clients’ business issues and the industries in which they operate.

• Conduct in-depth external research, including competitor organizational mapping, geographic talent availability, compensation benchmarking, and skill trend analysis across AEC and adjacent industries
• Identify emerging talent and capability risks and opportunities tied to the enterprise growth plan
• Build and deliver executive-ready narratives that combine internal signal with external market intelligence to inform workforce planning and business decisions
• Help to build bench strength for future leadership needs, identifying and nurturing high-potential external talent
• Execute best-in-class talent mappings for niche, competitive roles spanning technical disciplines, project leadership, and corporate functions
• Partner with sourcing teams, recruiters, TA leadership, and hiring leaders to translate business goals into targeted sourcing strategies and prospect management approaches
• Assist and actively participate in developing and maintain directional dashboards and talent visibility tools
• Leverage AI, LLMs, and automation to enhance research speed, personalization, and depth

Senior Talent Intelligence, Market Research Specialist

• 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.

Senior Clinical Research Associate

• Conduct in-depth fundamental equity research across assigned sectors and securities to identify investment opportunities and risks.
• Build and maintain detailed financial models, including forecasts for earnings, cash flow, and valuation metrics.
• Generate actionable buy, hold, and sell recommendations supported by clear investment theses and market analysis.
• Monitor earnings reports, industry developments, company news, and market trends to provide timely insights to portfolio managers.
• Manage a sector model portfolio and communicate portfolio strategy, positioning, and rationale to investment teams.
• Lead new investment idea generation and identify emerging opportunities within assigned sectors.
• Partner with portfolio managers and analysts to contribute to broader investment strategy and decision-making.
• Mentor and support associate analysts by reviewing research, providing feedback, and guiding professional development.

Equity Research Analyst, Health Care

• Oversee all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP Clinical SOPs.
• Conduct on-site and remote monitoring to ensure protocol adherence, maintain essential documentation, and keep site and patient data inspection-ready.
• Build strong relationships with sponsors and sites, serving as a key point of contact throughout the study.
• Support development of study-specific procedures (e.g., Monitoring Plans) and assist in training or coordinating other CRAs.

• Research criminal records in jurisdictions throughout the United States
• Report results according to Validity's formatting standards
• Ensure compliance with the Fair Credit Reporting Act
• Compile information from various research sources
• Follow local, state, and federal laws in reporting records
• Liaise with the Quality Assurance team

Research Specialist – Full-Time

• Conduct in-depth due diligence on investment management firms and multi-asset strategies
• Lead and/or participate in manager interviews with portfolio management teams and business leadership
• Perform qualitative assessment of investment teams and organizations
• Build and maintain analytical content across research deliverables
• Produce high-quality written research
• Contribute to post-meeting discussions and the development of recommended manager ratings
• Attend external conferences, as appropriate
• Provide ad hoc support to consultants in preparing for internal and external research meetings

Investment Research Specialist

• Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks
• Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities
• Assess investigational product through physical inventory and records review
• Documents observations in reports and letters in a timely manner using approved business writing standards
• Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution
• May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner
• Conducts monitoring tasks in accordance with the approved monitoring plan
• Participates in the investigator payment process
• Ensures a shared responsibility with other project team members on issues/findings resolution
• Investigates and follows-up on findings as applicable
• Participates in investigator meetings as necessary
• Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites
• Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted
• Performs trial close out and retrieval of trial materials
• Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations
• Conducts on-site file reviews as per project specifications
• Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required
• Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System)
• Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts
• Responds to company, client and applicable regulatory requirements/audits/inspections
• Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner
• Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members
• Contributes to other project work and initiatives for process improvement, as required

Clinical Research Associate II – Oncology, Ophthalmology

• Assist project teams in compiling and synthesizing information (e.g., conducting literature reviews and policy scans).
• Prepare and assist with primary source data collection through interviews, focus groups, and surveys; organize materials; and contribute to content development.
• Participate in the collection and review of research and evaluation data.
• Analyze quantitative and qualitative research data and contribute to the reporting and interpretation of findings.
• Prepare documents, portions of reports, briefs, charts, and graphs that describe and interpret findings of analyses.
• Support proposal writing and business development activities.
• Support project management tasks, including developing project timelines, coordinating meetings, and tracking project progress.

Research Associate, Healthcare Innovations

• Research changes to tax forms
• Interpret the tax code and regulation updates that drove those changes
• Provide guidance to programmers on updates needed to calculations based on research findings
• Test tax return calculations for accuracy, consistency, and usability
• Develop and update documentation to support the tax return calculations and other collateral
• Eventually lead or assist other leaders on team projects, as needed
• Provide support for the products we create through both direct and indirect communication channels

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Research Analyst – Non-Data

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Senior Clinical Research Associate – CNS/Rare Disease

Equity Research Specialist

Research Associate

Research Specialist

Research Analyst

Senior Market Research Consultant

Research Analyst

Senior Talent Intelligence, Market Research Specialist

Senior Clinical Research Associate

Equity Research Analyst, Health Care

Senior Clinical Research Associate

Research Specialist – Full-Time

Investment Research Specialist

Clinical Research Associate II – Oncology, Ophthalmology

Research Associate, Healthcare Innovations

Senior Tax Research Specialist