Research Analyst

• The Research Associate II, under general supervision, performs intermediate to advanced laboratory testing related to cell culture studies.
• This role supports daily culture operations, contributes to method development, and performs analytical testing and troubleshooting to ensure reliable experimental outcomes.
• The Research Associate II assists in project coordination and may train junior staff.
• Perform and optimize cell culture operations, including cryopreservation, thawing, expanding, maintaining, and banking mammalian and specialized cell lines with minimal supervision.
• Independently perform and optimize cell culture experiments such as batch, fed-batch, and/or perfusion.
• Scale-up cultures from flasks to bioreactors, such as shake flasks, spinner flasks, wave bags, or bench-top bioreactors.
• Monitor cell growth, viability, and productivity using analytical tools such as Vi-Cell, Cedex, Revvity.
• Analyze and interpret experimental data, prepare detailed technical reports, and present results in written or oral form to the project team.
• Write experimental protocols and SOPs.
• Identify, troubleshoot, and resolve routine technical issues while contributing to the improvement of protocols and workflows.
• Lead coordination efforts across the team to establish and maintain inventory systems, forecast consumable needs, and schedule equipment maintenance.
• Proactively identify bottlenecks in resource availability and recommend process improvements to enhance operational efficiency.
• Manage day-to-day responsibilities with a high degree of consistency and accuracy, anticipating workflow bottlenecks and reprioritizing as necessary to meet deadlines.
• Own documentation and record management for all cell culture activities, ensuring complete traceability and regulatory compliance.
• Contribute to the development, revision, and maintenance of SOPs by applying technical knowledge, hands-on experience, and process understanding.
• Train and mentor junior research associates by providing technical guidance, onboarding support, and feedback to ensure alignment with laboratory standards and best practices.
• Champion safety and compliance across cell culture operations by staying current with regulatory changes, recommending updates to SOPs, and mentoring team on best practices.

Research Associate II – Cell Culture

• Execute HEOR evidence generation tactics under minimal supervision and ensure the timely dissemination and communication of HEOR research
• Provide strategic input to support the pull through of evidence generated into publications and other promotional or reactive materials
• Present and discuss HEOR project methods and findings to diverse audiences
• Develop therapeutic area knowledge and expertise, and be able to engage with experts in the HEOR area for specific disease areas
• Appropriately select and manage vendors and resources, including submission of information for contracting and other internal processes and making sure projects are completed within timeline and allocated budget and met all compliance requirements
• Collaborate and partner cross functionally including with medical, commercial, policy, pricing, Squad teams, and across US market access and field organizations to provide strategic input in support of the development of US value propositions for specific products
• Own professional development and identify opportunities to develop leadership, strategic and technical skills
• Comply with all company policies and regulations

Associate Health Economics and Outcome Research Specialist

• 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

• Provide project management and logistical support for multiple research hubs and studies
• Support operations of complex research projects and assist in data management
• Build relationships with external collaborators and team members
• Maintain meeting agendas and follow up on action items
• Participate in research activities including developing protocols and conducting interviews
• Support project-related communication and deliverables
• Organize and execute project events and track project milestones

Research Associate

• Execute in vivo pharmacology studies including preparation (e.g. ear tagging, shaving)
• Adhere to institutional SOPs and IACUC protocols
• Upload and manage experimental data in vivarium management systems and ELN
• Write study protocols and graph data using Prism
• Prepare formulation buffers and compound dosing solutions for small molecules

Pharmacology Operations Research Associate – Contract

• 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

• 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

• Research state-level policies and Medicaid programs for target launch states, 6–12 months ahead of launch, to support the expansion roadmap
• Build and maintain a living state policy library - the authoritative internal reference for program eligibility, reimbursement structures, regulatory requirements, and operational implications by state
• Keep records current as policies evolve, and proactively surface changes that affect our roadmap or existing markets
• Research and maintain an ongoing record of competitors - their footprint, positioning, program participation, and strategic moves
• Surface competitive signals and market shifts to leadership through regular briefings
• Prepare and submit Medicaid applications to support market launches, on time relative to launch timeline gates
• Deliver structured launch readiness assessments for target states ahead of go/no-go decisions

Senior Associate, Research – Market Strategy

• Provides market research support in compiling and publishing high quality, comprehensive analysis and research on individual corporations, industries, financial markets, and economic developments as assigned.
• Expert level professional role requiring in-depth knowledge/expertise in own domain/field of specialty and working knowledge of broader related areas to run data analysis and develop research reports
• Solves complex problems requiring analysis of multiple variables, which may require consultation with multiple stakeholders
• Uses advanced methods to contribute to new solutions and recommend standards against which others will operate
• Interprets guidelines, standards, policies, and results of analysis to inform decision making at senior levels
• Builds stakeholder alignment in leading activities, identifying, and leading problem resolution

Equity Research Associate – Connectivity Semiconductors, Networking

• coordinate, schedule, and manage field research activities such as interviews, focus groups, and survey administrations;
• cultivate and sustain strategic partnerships with internal and external teams;
• assist with participant recruitment and incentive management.
• establish and maintain data collection and implementation measurement systems to monitor program quality;
• participate in or lead various data collection efforts (e.g., focus group, surveys, interviews, etc.);
• conduct user needs assessments and use data-driven frameworks to guide continuous product iteration.
• build, maintain, clean, and manage large datasets (e.g., Common Core of Data school directory files, client implementation databases, etc.) using Stata, R or another statistical software package;
• effectively summarize descriptive data for client products, dissemination, and annual reports.
• contribute to and/or lead the conceptualization and writing of small-to-large project reports and proposals;
• prepare descriptive reports, analytic sections, and evaluation reports;
• assist in the preparation and submission of large and small proposals.
• facilitate meetings and present research findings;
• interface with clients and lay persons related to data collection, analyses and reports;
• communicate effectively with a range of internal and external audiences including colleagues, clients, researchers, practitioners, and lay persons.

Quantitative Research Associate

• Oversee the operational aspects of clinical trial conduct at investigational sites to ensure data integrity, regulatory compliance, and adherence to Good Clinical Practice (GCP) guidelines.
• Support multiple clinical trials across various therapeutic indications and monitor site performance, resolving issues, and facilitating communication between sponsor and site personnel.
• Evaluate clinical trial resourcing requirements for qualification (SQVs), training (SIVs), monitoring (IMVs) and support of sites during the conduct of the trials.
• Work with multiple trial sites and multiple studies of varying indications simultaneously.
• Develop and maintain a monitoring plan for assigned clinical trial(s).
• Liaise with external clinic and/or hospital investigators and associated staff conducting the trial as required.
• Oversee the setup of the trial sites; ensuring each site has the appropriate trial materials to conduct the study.
• Oversee site activation process for each study.
• Periodically review data to identify potential issues or inconsistencies that could signal problems with data collection or monitoring.
• Track patient enrollment and recommend solutions to trial site staff to increase appropriate enrollment of qualified subjects.
• Provide support for the processing of data queries, deviations, adverse events, etc.
• Write monitoring visit reports.
• Develop and execute a plan to close trial sites on completion of the trial and perform associated close-out activities.

• Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance.
• Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials.
• Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience.
• 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 ongoing 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 – Eye Care, Specialty, Aesthetics

• Perform monitoring and site management work to ensure proper conduct of study protocols.
• Conduct site monitoring visits in accordance with contracted scope of work and Good Clinical Practice.
• Collaborate with sites to drive subject recruitment plans.
• Administer protocol training and establish lines of communication with sites.
• Evaluate the quality and integrity of study site practices.
• Track regulatory submissions and approvals, enrollment, and data query resolutions.
• Ensure site documents compliance with GCP and regulatory requirements.
• Create and maintain documentation regarding site management and monitoring visit findings.
• Liaise with study team members for project support.

Senior Clinical Research Associate, Sponsor Dedicated

• Collects, evaluates and/or abstracts clinical research data.
• May assist in designing forms for data collection/abstraction.
• Enters and processes clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
• Completes Case Report Forms (CRFs).
• Schedules research participants for research visits and research procedures. Provides supervised patient contact or independent patient contact for long term follow-up patients only.
• Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
• Assists with clinical trial budgets and patient research billing.
• Responsible for sample preparation and shipping and maintenance of study supplies and kits.
• Ensures compliance with protocol and overall clinical research objectives.
• Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
• Maintains research practices using Good Clinical Practice (GCP) guidelines.
• Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
• May serve as one point of contact for external sponsors for select trials. May respond to sponsor inquiries and attends meetings regarding study activity under the direction of supervising staff.

Clinical Research Associate I – Alzheimer’s and Dementia Program

• Obtain, organize, and analyze market-related equity information
• Work closely with the firm's portfolio managers
• Prepare and lead due diligence discussions and model-building

Equities Research Associate – Small Cap

• Conduct quantitative and qualitative research and author, co-author, and contribute writing and research to policy briefs, data tools, analyses, and articles.
• Develop and maintain Python-based workflows that automate data collection, cleaning, integration, quality assurance, and updates of large housing, demographic, economic, and geospatial datasets.
• Design, maintain, and document updates for the Partnership’s public-facing data tools, dashboards, and research products.
• Conduct quantitative and spatial analyses using Python, SQL, and/or GIS to evaluate housing affordability, housing need, preservation opportunities, and other policy issues.
• Contribute to the ongoing development of new quantitative and qualitative research methods to support our research agenda and in response to the needs of our partners.
• Respond to inquiries from government agencies, jurisdictions, nonprofit developers, and research institutions.
• Represent the Partnership through presentations to working groups, regional conferences, and other external settings.
• Provide data, technical assistance, and other information to the CEO and Director of Policy Advocacy to help the Partnership advance its policy agenda.
• Stay current with pertinent literature, developments, and data visualizations around issues of demographic change, housing supply, affordability, inequality, mobility, and equitable growth.
• Plan and execute segments of research/policy projects in consultation with and under the general supervision of senior staff.
• Perform routine administrative functions (e.g., submission of timesheets, participating in performance evaluations, etc.).

Senior Research Associate

• Conduct rigorous peer-reviewed quantitative research and analysis
• Leverage knowledge of portfolio optimization, trading strategies and portfolio analysis
• Deliver high-impact research on portfolio construction and optimization
• Develop and maintain relevant quantitative models and frameworks
• Partner with QRA leadership, Portfolio Strategy Management leadership, and Investment Group associates
• Work collaboratively with members of the QRA team
• Respond to deadline-driven requests requiring quantitative analysis
• Communicate results and recommendations in an appropriate format
• Help develop computing environments to support research

Quantitative Research Associate – Systematic Portfolio Construction

• Perform on-site and remote monitoring visits for assigned sites in accordance with the Clinical Monitoring Plan, ICH GCP guidelines, and applicable local regulations.
• Conduct source data verification to ensure Case Report Form (CRF) data is accurate, complete, and consistent with source documents and the protocol.
• Manage day-to-day communication with assigned sites, supporting enrollment, query resolution, and overall site performance.
• Proactively identify and document site level risks and issues, respond to study specific questions, and manage escalations through to resolution.
• Oversee the collection, review, and maintenance of essential regulatory and study documents to ensure inspection readiness.
• Collaborate closely with investigators and internal clinical teams to support effective study start up, conduct, and close out and to ensure successful trial execution.
• Oversee the execution of clinical trial activities in accordance with Good Clinical Practices.

Senior Clinical Research Associate – Temporary

• 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

• Manages 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.
• Mentor & manage junior researchers on the project execution & client management process.
• Bring an exceptional drive and entrepreneurial mindset, while also being highly organized related to planning and implementing both strategic and tactical project timelines.
• Be an enduring, positive and collaborative member of the team who genuinely cares about all facets of the company, our strategy and reputation in the market.

Research Analyst jobs in California

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Research Associate II – Cell Culture

Associate Health Economics and Outcome Research Specialist

Clinical Research Associate

Research Associate

Pharmacology Operations Research Associate – Contract

Research & Development Rotational Program Associate

Clinical Research Associate, Oncology

Senior Associate, Research – Market Strategy

Equity Research Associate – Connectivity Semiconductors, Networking

Quantitative Research Associate

Clinical Research Associate

Clinical Research Associate II – Eye Care, Specialty, Aesthetics

Senior Clinical Research Associate, Sponsor Dedicated

Clinical Research Associate I – Alzheimer’s and Dementia Program

Equities Research Associate – Small Cap

Senior Research Associate

Quantitative Research Associate – Systematic Portfolio Construction

Senior Clinical Research Associate – Temporary

Research Consultant

Senior Research Consultant