Research Scientist

• Assist the research coordinator (CRC/CCRC) in conducting clinical trials
• Establish good rapport with potential study subjects
• Collect clinical data, including vital signs, ECG recordings, height, and weight
• Collect and process laboratory specimens as needed
• Schedule study subjects for study visits
• Record and file clinical research data
• Maintain timely records of completed study visits and procedures in the organization’s Clinical Trial Management System
• Review and retrieve medical records

Assistant Research Coordinator

• Map and advance university and community-college partnership pathways for STEM education and workforce sponsored projects
• Coordinate with institutional sponsored programs, research development, and faculty PIs on roles, scopes, and proposal timelines
• Support research design, evaluation framing, and partnership documentation suitable for NSF-style and related education packages
• Facilitate introductions among K-14, community-college, industry, and university partners when the project design calls for it
• Contribute specialist qualifications and citeable past projects to WIL grant and sponsored-research packages when permissioned

University Partnership Liaison, Co-PI-ready Research Scientist

• Support data collection and management, data project timelines, technical infrastructure, and other data tasks for research cohort studies
• Assist in developing and coordinating data collection tools, including surveys and data collection forms
• Maintain project databases such as REDCap and Ripple or similar systems
• Support database creation, data problem identification and resolution, and results reporting
• Participate in data review, cleaning, and organization
• Develop programs supporting database creation, data problem identification and resolution, and results reporting
• Collaborate with internal staff and external study partners
• Attend and actively participate in staff, data/operations, and co-investigator meetings
• Provide support to internal and external data and project collaborators
• Perform day-to-day general tasks in support of research studies
• Contribute to maintenance of software applications and relevant data and technical documentation
• Perform other duties and projects as assigned

Senior Research Assistant

• Develop worldwide product regulatory strategies for assigned indications to optimize labeling and obtain the shortest time to approval
• Assess regulatory and competitive landscapes to establish global regulatory strategies that facilitate speed-to-market and targeted product labeling
• Provide expert advice as Global Regulatory Lead to Product Development Teams
• Serve as the regulatory point of contact for products within and external to GRACS throughout the drug life cycle
• Lead the Global Regulatory Team coordinating cross-functional regulatory support for development programs and marketed products
• Coordinate preparation, submission, and follow-up with regulatory agencies and subsidiaries for applications and submissions
• Conduct regulatory review and final approval of submissions and associated documentation
• Review and provide final approval of local registration study protocols when needed for marketing authorization in secondary markets
• Interact independently with regulatory agencies including FDA and EMA through meetings, teleconferences, and written communications
• Coordinate regional regulatory strategy and submissions with Regulatory Affairs Europe and local affiliate teams
• Review worldwide marketing applications, clinical study reports, protocols, and investigator brochures
• Prepare INDs/CTAs for global studies involving investigational drugs and biologics
• Participate in regulatory due diligence for licensing candidate reviews
• Independently manage complex projects as the accountable global point of contact

Principal Scientist, Regulatory Liaison – Immunology

• Lead the design, optimization, and application of experimental and computational workflows in human immunology and translational research
• Design, develop, and conduct research experiments
• Lead development and implementation of integrated single-cell workflows, including scRNA-seq, CITE-seq, BCR/TCR sequencing, and scATAC-seq
• Develop and optimize sample processing, cell isolation, sorting, fixation, and library preparation workflows
• Evaluate and implement single-cell, spatial transcriptomics, sequencing, and immune-profiling technologies
• Drive experimental platform development through experimentation, optimization, troubleshooting, and strategic planning
• Design and implement functional and mechanistic immune assays
• Develop perturbation strategies using CRISPR/Cas9, lentiviral approaches, RNA-based methods, or pharmacological modulation
• Investigate immune-cell activation, differentiation, exhaustion, memory, antigen specificity, and therapeutic responses
• Integrate multi-omics, immune-receptor, phenotypic, and functional assay data to identify mechanisms and biomarkers
• Partner with computational scientists on multi-modal datasets and reproducible bioinformatics and AI/ML workflows
• Collaborate with academic, clinical, and industry partners on assays, reagents, technologies, and translational research programs
• Lead studies involving human clinical specimens and preclinical models of HIV, cancer, infectious disease, and vaccine responses
• Oversee quality and training of team members; mentor postdoctoral fellows, graduate students, research scientists, and junior laboratory personnel
• Contribute to scientific strategy, NIH grants, collaborative proposals, manuscripts, presentations, and intellectual-property development
• Establish standardized, reproducible assay and data-generation protocols
• Assist with grant and funding applications and potentially serve as principal investigator on funded proposals with faculty approval

Academic Research Scientist – Pathology

• Design and refine data collection instruments, including semi-structured interview guides and surveys
• Conduct and facilitate virtual key informant interviews and group discussions with investigators, trainees, and implementation partners in diverse global settings
• Manage qualitative data in qualitative data analysis software, including transcript preparation, codebook development, and coding
• Build and apply codebooks using deductive and inductive approaches across data sources and cohorts
• Apply implementation science frameworks such as RE-AIM, CFIR, and PRISM to organize and interpret findings
• Design and implement implementation science training courses for adult learners using adult learning principles
• Provide mentorship and guidance to analytic staff
• Support large-group academic meeting coordination, including drafting agendas, polling questions, and meeting summaries
• Lead projects involving technical assistance, health policy or health care delivery model implementation, monitoring, program evaluation, and learning collaboratives
• Provide operational and scientific oversight for research projects, including serving as project director, deputy project director, or task lead
• Oversee individual and team tasks and timelines with a Project Manager
• Build and maintain relationships with project sponsors, external partners, internal managers, and staff
• Participate in proposals for new research and evaluation projects
• Contribute to study protocol development and analytic approaches
• Develop and conduct methodological and applied research leading to peer-reviewed publications, sponsor reports, and other dissemination strategies

• Prepare samples and perform analytical tests
• Record data and observations and prepare experiment summaries
• Perform compaction testing
• Analyze compacted samples for thermal conductivity, push-out strength, and X-ray results
• Troubleshoot basic process issues and escalate appropriately
• Perform parameter optimization and failure analysis
• Handle microscopic components using microscopes, tweezers, and vacuum tools
• Document processes, perform basic troubleshooting, and maintain repeatability and yield
• Contribute to development and improvement of chemical products and technologies
• Support new product development and continuous improvement initiatives
• Collaborate in multidisciplinary and cross-functional teams

R&D Scientist I

• Develop and benchmark novel agent architectures, reasoning strategies, and tool-use patterns for scientific research workflows
• Prototype agentic capabilities across drug discovery, clinical development, and translational science
• Rapidly iterate to identify approaches delivering genuine scientific value
• Partner with therapeutic-area researchers to identify high-impact research problems
• Translate domain expertise into concrete agent designs and experimental tool integrations
• Publish findings through peer-reviewed papers, demonstrations, and knowledge-sharing
• Establish patterns and reference implementations for moving successful innovations from experimentation into broader platforms
• Define criteria for production readiness without owning ongoing operations
• Contribute as an individual contributor and developing subject-matter expert in Data Science
• Develop actionable insights, methods, and research for the internal Data Science community
• Contribute to scientific projects, programs, and processes important to the Data Science function

Principal Scientist, DDSAI, AI/ML

• Design and execute in vivo pharmacology studies across Neurology programs in rodents and non-human primates toward IND submission
• Partner with toxicology and translational teams to ensure rigorous, reproducible, and translatable in vivo pharmacology data
• Inform dose selection and go/no-go decisions
• Develop and implement pharmacodynamic and efficacy assessments
• Troubleshoot assays and quality-control data from CROs and external partners
• Manage CRO relationships and monitor study progress
• Identify emerging study risks and present progress updates in team meetings
• Analyze in vivo pharmacology endpoints, including PK/bioanalysis and pharmacodynamic and/or efficacy endpoints

Principal Scientist, In Vivo Pharmacology, Neurology

• Design and conduct independent and collaborative research and evaluation studies supporting 988 Lifeline priorities
• Conduct quantitative and qualitative analyses using 988 Lifeline data, survey data, pilot data, and other relevant sources
• Analyze crisis service data to assess practices, outcomes, and opportunities for service improvement
• Design and support research, pilot studies, and evaluation activities using methods appropriate for crisis service settings
• Develop, refine, and evaluate surveys, measurement instruments, and other data collection tools
• Apply research frameworks and methods to assess effectiveness, feasibility, and quality of practices, interventions, and measures
• Support 988 departments in evaluation design, data collection, analysis, and interpretation of findings
• Maintain and update the biannual literature review, including evidence searches, study summaries, citation tracking, and synthesis of findings
• Prepare analytic summaries, reports, manuscripts, conference abstracts, presentations, briefs, and other dissemination materials
• Collaborate with Research and Evaluation colleagues, Lifeline departments, Data Analytics, Data Governance, and other internal partners
• Interpret findings considering operational context, research design, data quality, methodological limitations, and implications for practice
• Maintain transparent documentation of methods, analytic decisions, limitations, and findings
• Communicate status updates, analytic findings, limitations, risks, and potential roadblocks to the Lead Research Scientist