Research Analyst

• Support financial management of sponsored research programs, ensuring accuracy, timeliness, and compliance
• Prepare and analyze general ledger entries, account reconciliations, and budget-to-actual reports
• Assist with award setup in financial systems by coordinating documentation and collaborating with SPA
• Manage invoicing and accounts receivable (A/R) to ensure accurate billing and timely collections
• Develop and format financial reports and dashboards for internal leadership review
• Contribute to bi-monthly deficit reporting and support leadership decision-making
• Process journal entries, budget adjustments, and activity closeouts in alignment with sponsor timelines
• Maintain knowledge of sponsor regulations and institutional policies to minimize compliance risk
• Provide guidance and training to staff on financial reporting and systems

Research Financial Analyst II

• 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

• Orchestrate a highly relevant and impactful insight agenda for the US Systemic Mastocytosis business
• Be a highly valued strategic thought partner to the US Commercial team
• Effectively support / inform standard US Commercial business processes
• Cultivate strong partnerships across a matrixed internal environment
• Cultivate relationships with the Insights vendor community
• Effectively manage projects, driving collaboration between internal and external teams
• Communicate data / insights clearly and concisely

Associate Director, Market Research – Systemic Mastocytosis

• Design, manage, and govern the portfolio of advanced research and technology programs that translate Bose Research discoveries into scalable platform capabilities.
• Ensure that research programs are well-defined, strategically aligned, and executed with discipline.
• Partner with Franchise Architects and research leaders to translate long-term science arcs into clearly defined research programs.
• Implement a disciplined, phased funding model for research initiatives.
• Work closely with Bose-X and engineering teams to ensure successful transition of validated research capabilities into scalable platform components.
• Coordinate programs across multiple research franchises to ensure collaboration and avoid duplication.
• Provide clear visibility into program status, risks, and opportunities for senior leadership.

Associate Director, Program Portfolio – Research

• 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

• Formulate in-depth investment recommendations based on fundamental analysis, valuation and risk assessment across the emerging immunology landscape
• Collect and rigorously analyze data related to therapeutics and various diseases, including scientific papers, clinical data, and KOL perspectives
• Design and execute primary market research, including market surveys and expert interviews, synthesizing findings into differentiated investment insights
• Build, maintain, and refine financial models, including DCFs, probability adjusted revenue forecasts, and scenario analyses
• Author research reports, initiation notes, and company updates for distribution to Leerink Partners’ institutional clients and sales force
• Engage directly with institutional clients and internal stakeholders to communicate investment views and respond to market-driven inquiries
• Monitor news, data releases, and regulatory updates across the coverage universe, providing timely commentary to clients and the sales force
• Support senior equity analysts at medical and industry conferences

Equity Research Associate – Emerging Immunology

• 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 ICH-GCP, 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 & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
• Performs remote and on-site monitoring & oversight activities using various tools to ensure Data generated at site are complete, accurate and unbiased and subjects’ right, safety and well-being are protected.
• Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out 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 CRA-Manager, CRM, TA Head and CRD as needed.
• Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites.
• Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.
• Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor and sharing best practices as appropriate/required.
• Supports and/or leads audit/inspection activities as needed.
• Performs co-monitoring visits where appropriate.
• Following the country strategy defined by CRD and/or CRA-Manager, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities.

Clinical Research Associate, Oncology

• Conducts fundamental credit research on Fidelity’s insurance/reinsurance partners, bank and broker/dealer trading counterparties, and treasury relationships
• Performs credit analysis on potential and existing counterparties based on an assessment of financial strengths and weaknesses
• Prepares formal credit research notes on each counterparty, including the assignment of an internal credit rating
• Understands country, industry, market, economic, political, and regulatory issues relevant to the counterparty's credit profile
• Leads due diligence meetings with counterparty senior management teams
• Maintains relationships and clear communications with various internal stakeholders

Credit Research Analyst

• Provides market research support in compiling and publishing high quality, comprehensive analysis
• Integrates the broader organizational and industry context into advice and solutions
• Solves complex problems requiring analysis of multiple variables
• Uses advanced methods to contribute to new solutions
• Develops and maintains contact with market participants
• Conducts meaningful analysis at the functional or enterprise level

Equity Research Associate – Enterprise Software

• 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

• Provide guidance, oversight, and feedback to the CRA team to ensure adherence to project scope, SOPs, timelines, and budget requirements.
• Reviews monitoring visit reports, conducts co-monitoring and evaluation visits as needed.
• Ensures appropriate and timely investigator site visits.
• Coordinates with appropriate cross-functional departments to facilitate negotiation/issue resolution for clinical trial monitoring related issues.
• Assists in development of study-specific Monitoring Plans and training presentations as required.
• Performs qualification, initiation, interim, and close-out visits both remotely and onsite, ensuring proper documentation of monitoring visits.
• Maintains regular contact with study sites to ensure protocol/GCP compliance, assesses patient accrual rates, and responds to sponsor requests.

• Conduct literature reviews, evidence scans, environmental scans, and background research on gambling, gaming, digital dependencies, and related public health topics
• Support the development of annual reports, landscape analyses, policy briefs, surveillance products, and other research deliverables
• Assist with synthesizing, interpreting, and communicating findings from a variety of data sources
• Contribute to peer-reviewed manuscripts, conference presentations, technical reports, and other scholarly or applied research products
• Translate research findings into accessible materials for policymakers, healthcare providers, community organizations, and public audiences
• Create reports, fact sheets, presentations, infographics, and other knowledge-sharing resources
• Support emerging research priorities and special projects identified through stakeholder engagement, surveillance findings, and public health needs
• Maintain research resources, project documentation, references, dissemination materials, and tracking systems
• Collaborate with researchers, subject matter experts, academic partners, and community stakeholders to advance statewide research and public health initiatives
• Support stakeholder engagement, knowledge-sharing activities, and dissemination efforts across Massachusetts

• 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

• 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.

Research Analyst jobs in Massachusetts

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Research Financial Analyst II

Clinical Research Associate

Associate Director, Market Research – Systemic Mastocytosis

Associate Director, Program Portfolio – Research

Research & Development Rotational Program Associate

Equity Research Associate – Emerging Immunology

Clinical Research Associate, Oncology

Credit Research Analyst

Equity Research Associate – Enterprise Software

Senior Clinical Research Associate

Clinical Research Associate

Research Analyst

Research Analyst – Custom Market Research

Senior Research Analyst – Institutional Loans

Equity Research Specialist

Research Associate

Research Associate

Global Industry Analyst, Consumer

Research Specialist

Clinical Research Associate II