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 the design and execution of market research projects
• Analyze and report on market research projects
• Deliver actionable insights utilizing various brand measurement sources
• Provide ongoing consumer research expertise and consultation to internal partners

Principal Associate, Market Research

• Design, execute, and analyze complex experiments related to cell and gene therapy manufacturing.
• Develop and optimize cell culture and purification processes for clinical and commercial manufacturing.
• Collaborate effectively with cross-functional teams, including R&D, engineering, product management, and quality control, to ensure project success.
• Maintain detailed experimental records and generate comprehensive reports to communicate findings.
• Proactively identify and troubleshoot technical challenges, implementing innovative solutions to overcome obstacles.
• Stay abreast of the latest advancements in cell and gene therapy manufacturing technologies and industry trends.
• Operates within Fresenius Kabi Good Documentation and Good Laboratory Practices.

Associate Research Scientist, Cell & Gene Therapy

• 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.
• Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.
• 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.

Senior Clinical Research Associate – Ophthalmology

• 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

• 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
• Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards, 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 such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy
• Advanced level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities
• Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey
• Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance
• Possesses experienced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development
• May participate in global/local task forces and initiatives
• Responsible for activities as assigned by manager
• 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
• Advanced ability to think critically to resolve site risk signals while having robust understanding of site processes to drive study execution
• Ensures preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance using a customer centric approach
• Identifies, evaluates and recommends new/potential investigators/sites on an on going basis
• Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel
• Ensures audit and regulatory inspection readiness at assigned clinical site at all times
• Manages investigator payments as per executed contract obligations, as applicable

Clinical Research Associate II – Immunology

• Develop clinical trial budgets, including review of protocols and relevant documents to ensure that appropriate costs and allocation of institutional resources are fully captured in the budget.
• Work in collaboration with ancillary teams, departments, investigators, research staff, supporting administration, and sponsors/funding agencies to create complete, comprehensive, accurate and timely budgets.
• Ensure appropriate research rates are applied to study budgets.
• Independently develop, negotiate, and finalize budgets of moderate complexity with sponsors, academic sites, and other extramural funding sources to reach an agreement on budget and payment terms.
• Submit and maintain the budget and other financial information into OnCore Clinical Trial Management System (CTMS) to maintain proper reimbursement and revenue integrity.
• Perform pre-award quality assurance to verify completion of required elements prior to Medicare Coverage Analysis.
• Communicate and meet with stakeholders to facilitate ongoing budget discussions and provide updates to relevant parties.
• Use advancing knowledge to develop and disseminate clinical research education as needed in accordance with federal regulations, institutional policies, and specific protocol requirements.
• Apply knowledge of clinical research to provide recommendations and direction to clinical research teams to ensure budgetary compliance throughout all phases of the Clinical Trial Financials Lifecycle.
• Develop and support the formulation of program policies, procedures, and resources to establish and enhance clinical trial financials workflows.
• Provide excellent customer service while maintaining accurate results in a fast-paced, deadline-driven team environment.
• Engage in special projects and ad hoc duties as a member of the administrative team.

Clinical Trials Budget Specialist II

• Translates business requirements into business solutions;
• Acts as liaison between departmental leaders, staff and information technology staff to design and configure business solutions to ensure business requirements have been met.
• Works closely with stakeholders to define business requirements and with technical staff to develop solution alternatives and actively participates in defining objectives to support changing business needs and availability.
• Coordinates IT troubleshooting and day to day activities within the department to ensure seamless and minimal downtime of hardware, software and reporting requirements.
• May manage small to mid-sized projects/tasks and represent the department on larger enterprise-wide project teams.
• Creates and maintains project schedules by developing project plans and specifications, estimating time requirements, establishing deadlines, monitoring milestone completion, tracking all phases of the project product/service lifecycle, providing timely reporting of issues that impact project progress, coordinating actions, and resolving conflicts.
• Coordinates and conducts project team meetings regularly to review project deliverables and deadlines.
• Has knowledge and experience in the various techniques to elicit, analyze and communicate requirements within assigned functional areas.
• Establishes test plans, test cases and executes testing.
• Assists with end user training.
• Recommends information technology solutions to meet business needs and coordinates the planning, development, and implementation of these solutions.

Business Analyst II

• Investigate and recommend first- and third-party data sources, research partners, and data collection approaches for both qualitative and quantitative research
• Design and orchestrate research methodologies, including data collection plans, interview approaches, survey inputs, timelines, budgets, and risk mitigation plans
• Develop research hypotheses that align to the overall research story, including primary and secondary hypotheses, key questions to test, and themes to validate with executive sponsors and subject matter experts
• Analyze qualitative inputs to identify best practices, case examples, emerging themes, and executive-relevant implications
• Integrate quantitative analysis into research outputs to strengthen explanatory value, support findings, and create more compelling insight narratives
• Leverage Alexander Group benchmarks, market data, interviews, surveys, client experience, and secondary research to build well-supported perspectives on go-to-market trends and practices
• Design new research frameworks, models, and solution concepts that expand AGI intellectual property in relevant topic areas
• Connect new research frameworks to existing AGI methodologies, benchmarks, consulting experience, and subject matter expertise
• Develop deep subject matter expertise in multiple go-to-market topic areas, such as sales strategy, account management, customer success, revenue operations, sales compensation, marketing, service, AI-enabled commercial models, or industry-specific growth practices
• Translate research findings into practical recommendations that are innovative, business-relevant, and actionable for executive audiences
• Contribute to AGI intellectual property, including research reports, articles, white papers, client-ready frameworks, executive presentations, virtual roundtables, and other market-facing content
• Develop the core storyboard for research deliverables, ensuring the narrative is clear, compelling, logically structured, and executive-ready
• Own the creation of client-facing and publication-ready research materials in multiple formats, including PowerPoint decks, written reports, executive summaries, frameworks, case examples, and readout materials
• Prepare materials for executive sponsor reviews, internal research meetings, client readouts, and external-facing events
• Work closely with executive research sponsors, practice leaders, consulting teams, and other experts to incorporate feedback and tailor research outputs to business priorities
• Finalize high-quality materials with limited oversight, ensuring content is proofread, data is reviewed, charts are accurate, formatting is polished, and style is consistent with AGI standards
• Create research deliverables that balance analytical rigor, concise storytelling, and practical relevance for senior commercial leaders
• Prepare agendas for and lead research check-ins with executive sponsors, practice leaders, subject matter experts, and internal project teams
• Conduct executive interviews with external research participants, clients, and senior stakeholders
• Prepare for and present research readouts to clients and internal audiences, tailoring depth, emphasis, and language to the audience’s role, level, and business priorities
• Facilitate discussions that test hypotheses, surface executive insight, validate findings, and refine final research conclusions
• Communicate complex research findings in a clear, concise, and persuasive manner through both written and oral presentations
• Build trusted working relationships with internal sponsors, consulting teams, research participants, and senior client contacts
• Create detailed research project plans that include workstreams, milestones, owners, timelines, dependencies, and deliverable expectations
• Execute against project plans while adapting to roadblocks, scope changes, data limitations, and emerging research findings
• Identify potential issues early, develop mitigation options, and communicate risks or constraints to project leaders and sponsors
• Ensure timely completion of research deliverables while maintaining high standards for quality, rigor, and business relevance
• Mentor junior team members by expanding their research, analysis, storytelling, and project management capabilities
• Provide coaching, feedback, and development input to project leaders on team member strengths, growth areas, and training needs

Research Consultant

• 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.
• Assist Regulatory permit submissions for the BRC.
• Assist USDA guideline training for all BRC members.

Senior Research Associate

• 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

• 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 Analyst jobs in Illinois

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