Research Analyst

• 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

• 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

• 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

• The role is accountable for performance and compliance for assigned protocols and sites in a country.
• Under the oversight of the CRA-Manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally.
• Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.
• Actively develops and expands the territory for clinical research, finding and developing new sites.
• Participates in internal meetings and workstreams as SME for monitoring processes and systems.
• 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.
• Participates & 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 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 internally 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 strongly to CRA team knowledge by acting as process Subject Matter Expert (SME), sharing best practices, making recommendations for continuous improvement and providing training as appropriate/required.
• Supports and/or leads audit/inspection activities as needed. Following the country strategy defined by CRD and CRA-Manager, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities.
• Mentors / buddies junior CRAs on process/study requirements and performs co-monitoring visits where appropriate.

Senior Clinical Research Associate – Early Stage Development

• The role is accountable for performance and compliance for assigned protocols and sites in a country.
• Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company's policies and procedures, quality standards and adverse event reporting requirements internally and externally.
• Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.
• Actively develops and expands the territory for clinical research, finding and developing new sites.
• Participates in internal meetings and workstreams as SME for monitoring processes and Systems.
• 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.
• Participates & 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 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

• 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

• accountable for performance and compliance for assigned protocols and sites
• ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures
• acts as primary site contact and site manager throughout all phases of a clinical research study
• develops and expands the territory for clinical research, finding and developing new sites
• performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents
• conducts site visits and maintains clear, comprehensive and accurate visit & non-visit contact reports
• communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, regulatory documentation, site audits/inspections
• identifies, assesses and resolves site performance, quality or compliance problems

Clinical Research Associate – Immunology

• The role is accountable for performance and compliance for assigned protocols and sites in a country.
• Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally.
• Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.
• Actively develops and expands the territory for clinical research, finding and developing new sites.
• Performs remote and on-site monitoring & oversight activities 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, close-out visits.
• Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.
• 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.

Clinical Research Associate, Cardiovascular, Vaccine, Infectious Disease

• 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.
• Participates & 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, 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.

Clinical Research Associate, Cardiovascular

• 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

• 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

• Assists all stages of the market research project cycle, including designing and developing questionnaires and discussion guides
• Overseeing data collection & ensuring strict quality control
• Identifying and writing up analytical findings
• Visualizing and reporting quantitative and qualitative findings
• Report writing and taking deliverables to the next level
• Working with marketing research software packages
• Help to proactively nurture and develop strategic client relationships
• Work closely and effectively with team members across the organization
• Bring an exceptional drive and entrepreneurial mindset, while also being highly organized and detail orientated
• Be an enduring, positive, and collaborative team member

Research Consultant

• 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

• 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 Specialist

• Drives understanding and delivery of quality clinical research for all monitoring and site management activities
• Takes ownership to deliver upon near-term USO Clinical Development (CDO) goals, including successful delivery of studies within the clinical trial portfolio
• Delivers all relevant services/tasks in support of the planning and implementation of quality-driven clinical trials, in line with established targets and strategies
• Implements proactive risk identification and mitigation planning for assigned clinical trial sites
• Verifies safety reporting and the proper handling, monitoring and storage of trial products
• Ensures accuracy, validity and completeness of data collected at clinical trial sites
• Develops therapeutic area knowledge sufficient to support role and responsibilities
• Drives recruitment and retention strategies to support clinical trial sites to meet country enrollment and retention targets
• Participates in the preparation, conduct and follow-up of audit and inspection activities

• Support the day-to-day management of a media measurement panel, including executing regular operational processes
• Analyse data trends to identify issues and opportunities for improvement
• Investigate client queries and provide clear, timely responses
• Collaborate with internal teams to develop and improve workflows
• Support ongoing innovation by testing new panel features and processes

Research Analyst jobs in New Jersey

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Clinical Research Associate

Senior Validation Analyst, Clinical Research

Associate Director, Market Research – Systemic Mastocytosis

Senior Clinical Research Associate – Early Stage Development

Clinical Research Associate – Oncology

Clinical Research Associate, Oncology

Clinical Research Associate – Immunology

Clinical Research Associate, Cardiovascular, Vaccine, Infectious Disease

Clinical Research Associate, Cardiovascular

Credit Research Analyst

Associate Principal Scientist – Outcomes Research – Hematology

Research Consultant

Research Analyst – Custom Market Research

Investigative Research Analyst

Insurance Claims Data Analyst

Research Specialist

Clinical Research Associate

Research Analyst, Behavioral Panels