Research Analyst

• Lead computerized system validation (CSV) activities for regulated digital and AI applications throughout the SDLC
• Develop and execute validation deliverables including Validation Plans, Risk Assessments, IQ/OQ/PQ documentation (where applicable), test scripts, traceability matrices, and Validation Summary Reports
• Partner with Business Analysts, Quality Assurance, IT, vendors, and project teams to ensure systems meet business and regulatory requirements
• Review software requirements, functional specifications, design documentation, and change controls to ensure validation readiness
• Design, execute, and document risk-based testing strategies that demonstrate systems perform as intended
• Create and maintain validation evidence in accordance with internal procedures and regulatory expectations
• Support system implementations, upgrades, patches, and application enhancements
• Review and approve validation-related change controls and ensure ongoing compliance for validated systems
• Investigate test failures, identify root causes, and collaborate with technical teams to resolve issues
• Participate in internal audits, sponsor audits, and regulatory inspections by providing validation documentation and subject matter expertise
• Contribute to continuous improvement initiatives that enhance validation processes, testing efficiency, and compliance

Senior Validation Analyst, Clinical Research

• Conducting research into international legal services markets through face-to-face and virtual interviews, by email and online
• Assessing research results to compile rankings of the top legal practitioners
• Presenting findings as succinct, engaging and accurate written copy
• Identifying trends and developments in the legal markets we cover
• Generating new research leads and content ideas for the reports
• Evolving our research methodology to produce as comprehensive and accurate reflections of the legal market as possible

Associate Research Analyst – Lexology Index

• 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

• Develop & Execute Targeted Search Strategies
• Partner with Client Partners and Recruiters to define search objectives and develop targeted executive search strategies for retained search engagements.
• Design and execute research strategies that identify executive talent, competitive talent pools, and target organizations aligned with client objectives.
• Apply advanced research methodologies and creative sourcing techniques to identify and engage passive executive talent with minimal oversight.
• Leverage expertise in the biopharmaceutical industry to advise search teams on market dynamics, talent availability, and competitive landscapes.
• Conduct in-depth market, competitive, and organizational research to support executive search engagements and new business opportunities.
• Develop comprehensive market maps, organizational charts, succession pipelines, and executive talent landscapes.
• Monitor industry trends, company growth, financing activity, acquisitions, leadership changes, and emerging therapeutic areas to inform search strategy.
• Synthesize complex information into actionable insights and recommendations for Client Partners and Recruiters.
• Identify, evaluate, and prioritize executive leaders using advanced research methodologies, industry networks, and executive search technologies.
• Build and maintain relationships with executives to develop long-term market intelligence and talent networks.
• Serve as a trusted research advisor to Client Partners and Recruiters throughout each engagement.
• Proactively communicate market intelligence, search progress, and candidate insights.
• Recommend strategic adjustments to search strategy based on market findings.
• Escalate search challenges appropriately while maintaining exceptional internal client service.
• Demonstrate expertise across the biopharmaceutical value chain.
• Prepare executive candidate profiles, position specifications, market intelligence reports, organizational analyses, and client presentations.
• Coordinate research deliverables, interviews, client meetings, and project milestones to ensure timely execution.
• Maintain accurate and comprehensive documentation within Thrive in accordance with firm standards.
• Ensure the accuracy of candidate information, market intelligence, organizational research, compensation data, and executive movement within internal systems.
• Support business development by developing market maps, talent intelligence, competitive analyses, and search examples for proposals and client pursuits.
• Mentor Research Associates and junior team members, sharing expertise in executive search research, market intelligence, and project execution.

Senior Research Analyst – Biopharmaceuticals

• 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

• 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

• Serve as the primary point of contact between investigation sites and the sponsor for early development multi therapeutic clinical trials.
• Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out
• Ensure site compliance with ICH-GCP, SOPs, and regulations
• Maintain up-to-date documentation in CTMS and eTMF systems
• Support and track site staff training and maintain compliance records
• Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting
• Support subject recruitment and retention efforts at the site level
• Oversee drug accountability and ensure proper storage, return, or destruction
• Resolve data queries and drive timely, high-quality data entry
• Document site progress and escalate risks or issues to the clinical team
• Assist in tracking site budgets and ensuring timely site payments (as applicable)
• Collaborate with cross-functional partners including CTAs, LTMs, and CTMs

Clinical Research Associate

• Develop and execute the HEOR strategy for Braeburn’s product(s), ensuring alignment with medical, brand, and market access objectives.
• In partnership with external and internal stakeholders, design, lead, and manage HEOR studies and projects, which may include retrospective database and claims analyses, real-world evidence (RWE) studies, patient-reported outcomes (PRO) research, burden-of-and cost-of-illness studies across various settings including institutional settings.
• Lead the development and updates of economic models-building, commissioning, or overseeing cost-effectiveness, budget impact models, and cost-offset analyses- and translate HEOR findings into payer, public sector, and policymaker value propositions, AMCP dossiers, value communication tools, and objection-handling resources.
• Manage external vendors, consultants, and academic collaborators, overseeing scope, budget, timelines, and the quality of deliverables.
• In close partnership with Scientific Communications, disseminate evidence through peer-reviewed publications, scientific congress abstracts and posters, and internal and external presentations.
• Serve as the HEOR subject-matter expert for cross-functional teams and, as requested, in external interactions with payers, institutional and public health agencies, policymakers, and key opinion leaders.
• Gather and synthesize insights and monitor the external OUD, addiction medicine, behavioral health, and criminal justice landscape to anticipate evidence needs.
• Ensure all HEOR activities comply with applicable scientific standards and legal, regulatory, and compliance requirements.
• Identify and pilot opportunities to apply AI/ML to improve the speed, scale, and rigor of evidence generation and synthesis.

Associate Director, Health Economics – Outcomes Research

• planning/managing of real-world evidence and non-interventional research activities for in-line and pipeline products in hematology
• support critical assessments of drivers and barriers to reimbursement and market access
• collaborate with internal teams and external partners, design non-interventional and data synthesis studies
• author study protocols, develop measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and publications
• hold responsibility for study-related contracting, budgets, and vendor/partner management
• develop American Managed Care Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers
• support local/regional country affiliates to understand local evidence generation needs
• work closely with cross functional teams to effectively communicate real-world evidence and non-interventional research activities internally and to external stakeholders
• maintain awareness of new scientific and methodological developments within therapeutic area and in outcomes research field
• build partnerships with scientific experts worldwide
• present outcomes research data at national and international congresses and publish articles in scientific journals

Associate Principal Scientist – Outcomes Research – Hematology

• Delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders
• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; participation in preparation and review of study documentation and feasibility studies for new proposals as required
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
• Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements

Clinical Research Associate, Histologist

• Lead quantitative and qualitative underwriting of investment managers, including evaluation of performance drivers, portfolio construction, risk management, and process consistency.
• Conduct operational due diligence across business operations, compliance frameworks, valuation practices, technology infrastructure, and service providers.
• Support portfolio construction and manager implementation within a multi-asset OCIO framework.
• Maintain ongoing monitoring of approved managers through formal reviews, event-driven reassessments, and watch list oversight.
• Prepare investment committee materials, manager evaluations, scorecards, and strategic recommendations.
• Collaborate with internal investment, portfolio management, risk, compliance, and client teams.
• Mentor junior analysts and contribute to the ongoing enhancement of research frameworks and due diligence processes.
• Serve as a recognized subject matter expert across traditional asset classes, delivering internal investment updates, client presentations, market outlooks, and strategic positioning insights.
• Act as a market strategist within assigned asset class coverage, maintaining differentiated perspectives on macroeconomic conditions, valuation environments, and market cycles.
• Translate market developments into actionable manager research themes and investment recommendations for internal stakeholders and clients.
• Demonstrate expertise through published market commentary, white papers, presentations, or a track record of influencing investment outcomes.
• Represent the firm externally as a trusted investment strategist and thought leader.

• 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 technical and research support to update UPENN ration balancing
• Expand and update a dairy decision tool suite incorporating on-farm production data
• Develop and launch a benchmarking tool for PA dairy farmers
• Investigate and apply new non-linear programming technique to existing tools
• Re-launch and modernize dairy decision dashboard program
• Development of crop optimization tool and economic opportunity program
• Develop robotic feeding optimizer program
• Perform additional duties as assigned

Research Specialist

• Support a team of Investigators by conducting extensive research across multiple sources and tools.
• Research companies and individuals for case development using various investigative mediums.
• Conduct confidential background and due diligence investigations.
• Manage a large caseload and attorney requests in a dynamic and fast-paced environment.
• Collaborate with team members to support high-priority requests and cases.
• Assist with special projects as needed as an integral member of the Investigative Services Team.

Investigative Research Analyst

• Develop and maintain control structures to ensure data accuracy and quality across upstream and downstream systems
• Conduct data integrity gap analyses and partner with business and IT teams to resolve discrepancies
• Prepare monthly and quarterly claims analytics reports for leadership
• Analyze key performance indicators and support data‑driven decision‑making across the Claims organization
• Support fraud detection, subrogation analysis, medical management reviews, and legal analytics
• Collaborate with business stakeholders to understand requirements and develop tailored data solutions
• Present findings in a clear, concise, and visually compelling format

Insurance Claims Data Analyst

• 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 Analyst jobs in Pennsylvania

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Senior Validation Analyst, Clinical Research

Associate Research Analyst – Lexology Index

Clinical Research Associate – Oncology

Senior Research Analyst – Biopharmaceuticals

Clinical Research Associate, Oncology

Senior Research Analyst

Clinical Research Associate

Associate Director, Health Economics – Outcomes Research

Associate Principal Scientist – Outcomes Research – Hematology

Clinical Research Associate, Histologist

Senior Research Analyst

Research Analyst – Custom Market Research

Research Specialist

Investigative Research Analyst

Insurance Claims Data Analyst

Research Specialist