Research Analyst

• Provide support to the Head of Institutional Loans to build and manage a portfolio of institutional loans.
• Identify appropriate investment opportunities based on credit fundamentals of the issuer & sector and the bank’s credit risk appetite.
• Monitor the portfolio closely for financial & business updates and make timely buy, sell, hold recommendations.
• Work and present credits independently with minimal supervision and collaborate with the business, credit, internal audit and back office for credit approvals.
• Interact with senior management of portfolio companies & sponsors for investment diligence.
• Present new & existing credits at various credit committees at the bank.
• Provide on the job training in underwriting to junior members.
• Lead and/or participate in various technology & portfolio management projects.

Senior Research Analyst – Institutional Loans

• 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

• Assist with survey design, questionnaires, and sampling to meet client objectives
• Act as the day-to-day contact for clients and project collaborators
• Coordinate and manage multiple projects at once, ensuring on-time and accurate delivery
• Partner with suppliers when needed to ensure high-quality data collection at reasonable costs
• Analyze and interpret final datasets, creating clear, visually engaging reports (PowerPoint or similar)
• Guide clients through findings using YouGov’s analytics tools and software

Research Associate

• Conducting research and making investment recommendations within the Apparel & Retail industry
• Generating superior investment returns through fundamental company, sector and industry research and analysis
• Influencing portfolio managers with investment insights

Global Industry Analyst, Consumer

• 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

• 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.
• Conduct site evaluation, training, routine, and site closure monitoring activities with compliance to the protocol and monitoring plans, 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 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.
• Mentor and train less experienced CRAs on various aspects of work and provide input into their development.
• 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 using a customer centric approach.
• Identify, evaluate and recommend new/potential investigators/sites on an ongoing basis.

Clinical Research Associate II

• 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

• 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.

Senior Clinical Research Associate

• Drafts project deliverables, interacts with clients, and contributes to strategic thinking under the direction of senior staff
• Supports scientific coordination and project management
• Develops scientific deliverables (e.g., protocols, reports) under oversight of senior staff
• Participates in scientific guidance/consultation on project design and conduct
• Leads on or oversees development of project deliverables for senior review
• Interacts directly with project sponsors, physician experts, and clinical sites
• Assists in monitoring project budget spend and managing timelines for scientific tasks/deliverables
• Participates in development of abstracts and manuscripts
• Contributes to business development activities, including support of proposal development

Research Associate III – Real-World Science, Epidemiology, Scientific Affairs – Pregnancy Studies

• Develops study documents and tools, including Informed Consent Form (ICF) templates (for both local and central IRBs), site binder contents, etc.
• Supports sites in obtaining IRB approval, developing submission materials, and creating site-specific ICFs
• Responds to sites’ regulatory board requests for protocol and ICF clarification as needed
• Ensures all required site regulatory documents and approvals are in place prior to investigational product shipment
• Ensures all regulatory documents are collected and filed appropriately at both the site and in the Trial Master File (TMF); conducts routine file reviews
• Analyzes site performance problems (protocol adherence) and identifies solutions; provides ongoing training for study sites
• Maintains regular communication with study sites to ensure protocol/GCP compliance, assesses subject accrual rates, and responds to sponsor requests
• Conducts remote review of data entered on electronic Case Report Forms (eCRFs)
• Works closely with field CRAs and data management to resolve queries on discrepant data
• Assists with efforts to recruit investigative sites to participate in clinical studies
• Complies with ICH GCP guidelines, FDA regulations, and company SOPs
• Participates in internal, client/sponsor, scientific, and other meetings as required
• Manages and resolves conflicting priorities to deliver on commitments
• Performs additional duties as assigned

In-House Clinical Research Associate – 2

• Manage and support clinical sites from site approval through close-out
• Develop study documents and tools, including Informed Consent Form (ICF) templates
• Support sites in obtaining IRB approval and developing submission materials
• Respond to sites’ regulatory board requests for protocol and ICF clarification
• Ensure all required site regulatory documents are in place prior to investigational product shipment
• Conduct routine file reviews and analyze site performance problems
• Maintain regular communication with study sites to ensure compliance
• Conduct remote review of data entered on electronic Case Report Forms (eCRFs)
• Assist with efforts to recruit investigative sites to participate in clinical studies
• Comply with ICH GCP guidelines and FDA regulations
• Participate in internal, client/sponsor, scientific, and other meetings as required
• Manage and resolve conflicting priorities to deliver on commitments

In House Clinical Research Associate

• 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

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work, Alira Health SOPs and regulatory requirements
• May perform Central Monitoring activities, or act as the primary liaison between site and Central Monitor
• Collaborate with cross-functional teams and CRAs to maintain high standards of clinical trial conduct
• Conducts investigational product (IP) inventory and accountability, while evaluating storage conditions and access protocols
• Confirms IP has been dispensed and administered to participants in compliance with the study protocol
• Leverages expertise in GCP, local regulations and Alira Health procedures
• Reviews the Investigator Site File (ISF) for audit readiness including accuracy and completeness
• Reconciles the ISF with the Trial Master File (TMF)
• Performs quality checks on regulatory documents per ALCOA+ principles
• Supports audit readiness by submitting documents to the TMF
• Verification and review of safety events
• Prepares accurate monitoring visit reports and communication logs in alignment with Alira Health SOPs and the Clinical Monitoring Plan timelines
• Participants in internal, client/sponsor, scientific, and other meetings as required
• Oversees Clinical Research Associates (CRAs) to ensure monitoring visits are conducted within the timelines specific in the Clinical Monitoring Plan
• Monitors site and CRA performance to maintain SDV rates within study goal range
• Works closely with Project Managers, CRAs and Data Management to resolve CRF queries on discrepant data

Lead Clinical Research Associate

• Work with portfolio management, research, and business development teams to identify opportunities where AI can enhance alpha generation, portfolio construction, risk management, predictive analytics, and client-facing workflows
• Translate ambiguous investment problems into well-scoped technical solutions
• Work with central AI and engineering teams to productionize models and deploy them into investment workflows
• Help drive adoption of AI tools by communicating results clearly and enabling investment teams to use what you build
• Contribute to defining and articulating a firm-wide AI strategy for investment management

AI Research Analyst – AI, Digital Asset Solutions

• Communicate with the investment team to determine relative value, as well as communicate current views.
• Collaborate with the team to develop, articulate and implement strategic and tactical recommendations.
• Publish research papers for both internal and external use.
• Participate in presentations to clients and investment consultants.

Senior Research Analyst, Municipal Bonds

• Lead design and execution of equity‑centered RWD/RWE projects by therapeutic area that quantify disease burden, access, testing, treatment patterns, and outcomes across under‑represented populations.
• Develop mixed‑methods studies (EHR/claims analyses, registry data, SDoH integration, patient surveys, and qualitative interviews) and ensure outputs are timed to inform clinical programs, as well as relevant policy and commercial colleagues.
• Work cross-functionally to develop study protocols, statistical analysis plans, and methodological approaches that address selection bias, missingness in race/ethnicity/SDOH variables, causal inference, and subgroup inference.
• Integrate policy analysis into evidence generation: identify policy levers (e.g., Medicaid policy, payer coverage, reimbursement pathways) and translate study findings into policy recommendations.
• Manage strategic external collaborations and vendor relationships: identify and evaluate data partners, MSIs, FQHCs, safety‑net hospitals, community‑based organizations.
• Co‑lead co‑development of primary research with external partners (MSIs, FQHCs, community organizations) to ensure non‑extractive, trust‑based engagement and sustainable relationships that support recruitment and retention and post‑study continuity of care.
• Work closely with embedded/internal cross-functional partners to translate evidence into protocol design recommendations, site selection guidance, eligibility optimization, and outreach strategies.
• Produce actionable deliverables: TA‑specific, equity-centric RWD/RWE publications and plain language summaries and dissemination materials for both scientific and non‑technical audiences.
• Present findings to internal forums and to external stakeholders; publish in peer‑reviewed journals and present at scientific conferences.
• Mentor and build capacity across the HER Champion community; contribute to HER learning materials, SharePoint resources, and training modules.
• Ensure research adheres to ethical standards, privacy/regulatory requirements (HIPAA/GDPR where applicable), and community engagement best practices.

Health Equity Research Associate Director

• Conducts defined steps of an established search strategy by applying specified screening criteria and extracting required data to meet the objectives of a targeted literature review
• Drafts, revises, and quality checks study documents by using approved templates and incorporating direction from project leadership to align content with study scope and requirements
• Completes required training and conducts high-quality qualitative interviews with research participants (e.g., patients, caregivers) virtually or in person (travel required), adhering to the interview guide and study protocol
• Codes and analyzes qualitative participant-level data by applying a coding framework developed with guidance and oversight from the project lead
• Executes defined steps of survey implementation and analysis by conducting pilot testing, quality checking survey data, analyzing open-ended items qualitatively, and producing descriptive analyses
• Attends select client meetings (primarily virtual and occasionally in person) and captures discussion points, decisions, and next steps by producing clear, complete meeting minutes
• Drafts assigned portions of client deliverables (e.g., introduction, methods, and results sections) for presentations, reports, and memos by following guidance from the project lead
• Operates within the PCO Quality Management System by following standard operating procedures, including using the QC checklist to reduce errors before deliverables are finalized
• Delivers assigned tasks across multiple concurrent active projects by confirming requirements with project leads, managing personal deadlines, and communicating status to maintain project momentum

• Focus on alpha generation through differentiated fundamental research
• Operate primarily as a generalist across sectors
• Join a highly collaborative investment environment
• Contribute meaningfully to idea generation and security selection

Equity Research Analyst

• Conduct independent and collaborative research on oxygen dynamics in seawater, including analysis of triple oxygen isotope composition of dissolved oxygen.
• Design, develop, and optimize systems for the extraction of dissolved oxygen from seawater samples.
• Perform and refine quantitative reduction of oxygen to water for downstream isotopic or chemical analysis.
• Lead and contribute to the development, calibration, and testing of a prototype system for at-sea measurements of triple oxygen isotopic composition of dissolved oxygen.
• Analyze complex datasets and interpret results in the context of physical, chemical, and biological oceanographic processes.
• Prepare manuscripts, reports, and presentations for scientific publication and dissemination.
• Collaborate with interdisciplinary teams across WHOI and external partners.

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Senior Research Analyst – Institutional Loans

Equity Research Specialist

Research Associate

Research Associate

Global Industry Analyst, Consumer

Research Specialist

Clinical Research Associate II

Research Specialist – Legislation Specialty

Senior Clinical Research Associate

Research Associate III – Real-World Science, Epidemiology, Scientific Affairs – Pregnancy Studies

In-House Clinical Research Associate – 2

In House Clinical Research Associate

Investment Research Specialist

Lead Clinical Research Associate

AI Research Analyst – AI, Digital Asset Solutions

Senior Research Analyst, Municipal Bonds

Health Equity Research Associate Director

Research Associate

Equity Research Analyst

Research Associate III – MC&G