Top Research Associate Jobs

Implements and manages technical aspects of research projects, plans and coordinates project activities, collects and communicates data, liaises with clinical staff, ensures patient safety and regulatory compliance, mentors new staff, and participates in hospital initiatives.

Perform and analyze bioassays (cell-based assays, ELISAs), run plate-reader and flow cytometry assays, maintain multiple cell lines aseptically, troubleshoot experiments, record data per cGMP/GLP/GCP, and communicate results in notebooks and presentations.

Designs and executes in vitro cell-based assays for skincare ingredient discovery, maintains mammalian cell banks, performs ELISA/flow cytometry/qPCR and high-throughput sample workflows, analyzes and records data in electronic lab notebooks, and contributes to assay development and validation.

Lead on-site clinical monitoring and site management for oncology studies, ensuring protocol compliance, informed consent, data integrity (CRF review/query resolution), SAE reporting, registry management, initiation and close-out visits, vendor liaison, training/co-monitoring, and acting as local project coordinator. Significant travel to study sites required.

Provides scientific, technical, and people leadership for sterile liquid dosage-form and eyecare product formulation, process, analytical-method development, technology transfer, regulatory submissions, and commercialization. Leads development strategies, CMC activities, CRO and CMO partnerships, scale-up, and lifecycle management. Applies Quality by Design and statistical experimentation, interprets global GMP and CMC requirements, authors technical and regulatory documents, and supervises scientists while fostering scientific rigor, quality, safety, and collaboration.

Work with senior analysts to evaluate cancer immunotherapies via primary scientific, clinical, commercial, and financial analysis. Maintain trial databases, build and update financial and simulation models, write research reports, monitor regulatory and scientific developments, support conference work, and respond to internal and client inquiries.

Lead site management and monitoring for Oncology clinical trials (Phase I/early development), ensuring data integrity, subject safety, inspection readiness, TMF reconciliation, KRI monitoring, CAPA implementation, site activation and training, and oversight/mentoring of CRAs while supporting regulatory inspections and fostering key site relationships.

Execute bioanalytical tests (HPLC, SDS-PAGE, SDS-CGE, ELISA, UV-Vis) and basic biophysical characterization, perform elementary data analysis and troubleshooting, maintain lab and electronic notebooks, uphold instrument knowledge and lab safety, and contribute to contracted analytical projects under manager supervision.

Hands-on lab role to engineer stable mammalian cell lines (lentiviral transduction, CRISPR knock-ins/outs), run and optimize cell-based immunoassays (flow cytometry, ELISA, Incucyte), perform reagent and cell line qualification, analyze datasets, and present technical reports to support immuno-oncology drug discovery and development.

Coordinate and conduct field research including plot setup, seed preparation, planting, data collection, plot maintenance and harvest. Maintain and repair research equipment, manage warehouse tasks and shipments, prepare data reports, supervise staff and travel overnight to outlying sites.

Senior Research Associate responsible for designing, executing, and optimizing antibody binding and functional serology assays (ELISA, Luminex, MSD, Octet), performing epitope mapping and cell-based assays, maintaining mammalian cell culture, analyzing data (GraphPad Prism), documenting experiments in electronic lab notebooks, supporting assay automation and AI-enabled workflows, and collaborating across teams to advance preclinical through IND-enabling studies.

The Clinical Research Associate will manage study maintenance and closeout activities, liaise with study teams and external partners, and monitor clinical data and safety metrics.

Operate and improve an in-house AAV vector core: run weekly AAV production from cell culture through purification, perform QC assays (titer, purity, genome integrity), maintain ELN lot records and inventories, follow and update SOPs, troubleshoot production issues, and coordinate handoffs with program teams to ensure consistent, high-quality vectors.

As a Senior Researcher at WireScreen, you will develop data collections, analyze documents, and collaborate with teams to enhance intelligence platforms focused on global supply chains and compliance.

Manages commercial real estate data portfolios by conducting 50+ daily calls, investigating listings and transactions, validating AI-assisted research, and resolving data quality issues. Builds relationships with brokers, owners, developers, and investors while supporting client onboarding, product adoption, listing performance reviews, and training. Analyzes market trends and collaborates with regional teams to improve coverage, accuracy, and client value.

Conduct hands-on laboratory experimentation, product prototype preparation, simulations, and consumer research activities for wipes product development. Independently execute established methods, document and communicate results, investigate unexpected findings, recommend next steps, and support new techniques and process improvements. Teach less-experienced team members, manage lab supplies and maintenance, and ensure quality and safety compliance. Collaborate with project teams under supervision while contributing to regional and global initiatives.

Conduct industry and company-specific equity research for SMid Biotech: model financials, perform valuations, analyze filings and news, write research notes and sector reports, communicate with clients and management, and support Sales and Trading with market intelligence.

As a Clinical Research Associate, you will monitor clinical trial sites, ensure protocol compliance, manage study progress, and mentor staff.

Conduct monitoring and site management activities to ensure compliance with study protocols, manage progress of studies, and communicate effectively with sites.

The Clinical Research Associate will conduct monitoring visits, ensure compliance with study protocols, manage site communications, and support regulatory submissions and study management.

Monitor early-stage (Phase I) clinical trials: conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; resolve data queries; collaborate with investigators and prepare/review study documentation including protocols and clinical study reports.

Conduct and analyze specialized experiments bridging computational biology and wet-lab work. Analyze multi-omics sequencing datasets, develop computational workflows (R/Python/GitHub), assist manuscript and grant preparation, perform wet-lab tasks (library prep, PCR, flow cytometry, histology), operate complex equipment, and adhere to institutional research standards.

The Research Associate 1 supports laboratory experiments in myeloma research, conducting data analysis, reviewing literature, and assisting with manuscripts and database management.

Support senior analyst with company and industry research; build financial models and valuations; write company and industry reports; develop investment recommendations; engage company management, attend conferences and roadshows, and market research to sales and institutional investors.

Lead on-site clinical monitoring and site management for oncology trials including initiation, routine monitoring, close-out, SAE reporting, CRF review and query resolution, registry management, feasibility, training, and local coordination. Requires frequent travel and use of electronic data capture systems.