Top Research Associate Jobs

Execute and optimize immunoassay workflows on high-throughput, semi-automated platforms, process clinical samples, maintain and calibrate lab equipment, manage data and supplies, troubleshoot assays, and support grant material preparation while collaborating across assay development, platform, and product teams.

Conduct site qualification, initiation, monitoring, management, and close-out visits to ensure protocol, regulatory and ICH/GCP compliance. Review source documents and CRFs, manage queries, investigational product handling, ISF/TMF reconciliation, documentation, and support audit readiness. Act as liaison with sites and sponsors, support recruitment/retention, and may train junior staff. Heavy travel (up to 75%).

The Senior Clinical Research Associate will monitor clinical sites, ensure compliance with protocols, and collaborate with site staff to support trial execution.

Lead on-site clinical monitoring for oncology/hematology trials: conduct site selection, initiation, routine and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor patient safety and AE/SAE reporting; oversee drug accountability, support recruitment and retention, resolve data queries, track site budgets, and escalate risks to clinical teams while collaborating cross-functionally.

Serve as primary contact between investigational sites and sponsor; conduct site visits (selection, initiation, routine monitoring, close-out); ensure ICH-GCP and regulatory compliance; maintain CTMS and eTMF documentation; monitor patient safety and AE/SAE reporting; support recruitment, drug accountability, data quality, site training, budgets, and escalate risks to clinical team.

The Clinical Research Associate will conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with site staff and investigators.

Serve as primary contact between investigational sites and sponsor to conduct site selection, initiation, routine monitoring, and close-out. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety (AE/SAE/PQC), support recruitment and drug accountability, resolve data queries, track site training and budgets, escalate risks, and collaborate with cross-functional clinical teams.

Serve as primary site contact and perform site selection, initiation, routine monitoring, and close-out visits. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety and reporting, support recruitment and drug accountability, resolve data queries, track site budgets/payments, and escalate risks while collaborating with cross-functional clinical teams.

The Associate Analyst role involves analyzing industries, researching and assessing companies, building financial models, and contributing to investment decisions in a collaborative environment over a 3-year period.

The Strategy and Research Associate will conduct research and analysis, manage regulatory filings, and produce clear documentation for new products and initiatives at an automated insurance company.

Perform routine QC testing and documentation for protein, peptide, and antibody products (concentration, SDS-PAGE, endotoxin, TOC, conductivity). Support instrument calibration, lab maintenance, reagent preparation, inventory monitoring, peer review of records, and participate in lab meetings and continuous improvement initiatives.

Support the Managed Assets Research department in delivering high-quality investment solutions through research, communications, and client portfolio reviews.

Support Senior Analyst covering semiconductor companies by performing financial modeling, forecasting, valuation, industry data collection, and maintaining databases. Produce charts, written research, and presentations translating quantitative conclusions for clients. Balance heavy modeling periods with qualitative writing and presentations, collaborating with sales, trading, and company contacts to support published equity research.

Execute experiments, document findings, analyze data, optimize workflows, and contribute to genomics sample prep applications in a collaborative lab environment.

Analyze federal and state political, legislative, and regulatory developments to forecast market and company impacts. Produce internal research, present findings, collaborate with research, portfolio, and governance teams, engage subject-matter experts and policy contacts, and inform investment decisions.

Monitor and support clinical trials through site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; resolve data queries; collaborate with site staff and contribute to study documentation and reports.

Serve as primary site contact for early-development Phase I/II trials. Conduct site selection, initiation, routine monitoring, and close-out visits. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor safety reporting, support recruitment and drug accountability, resolve data queries, escalate risks, and coordinate site budgets and cross-functional teams.

Hands-on role producing and characterizing medium-to-large scale proteins for structural biology and drug discovery. Perform multiple purification methods (FPLC, affinity, ion-exchange, SEC, magnetic beads), run QC assays (SDS-PAGE, fSEC, DSF, flow cytometry), collaborate with discovery teams, maintain documentation, and prioritize reagent delivery timelines.

Perform quantitative ecology research: collect and analyze field and lab data, write code for data wrangling and analyses, collaborate on lab projects, and prepare reports or publications of findings.

The Clinical Research Associate performs site monitoring and management to ensure compliance with study protocols and regulatory requirements, tracks study progress, and facilitates site communication.

The Clinical Research Associate performs monitoring and site management to ensure regulatory compliance and data integrity in clinical studies.

Manage social science research projects and grants, including planning, data collection (surveys, focus groups, interviews), quantitative and qualitative analysis, visualization, reporting, client communication, IRB compliance, budgeting, and supervising student research staff to deliver timely project results.

Conduct fundamental equity research on connectivity semiconductors and networking companies: build and maintain financial models, produce research reports, perform valuation and forecasting, liaise with market participants, support senior analysts, and contribute to client-facing presentations and recommendations.

Manage and maintain research databases, create and run data queries, prepare reports, perform data migration and quality review, conduct chart abstraction, coordinate study activities including patient scheduling and specimen collection, and provide administrative support for clinical research studies.

Support protein engineering and binder discovery using display technologies. Design and generate libraries, perform NGS and flow cytometry-based selection, culture engineered yeast, construct immune repertoires, troubleshoot and optimize lead molecules, and maintain data quality in a lab-focused, on-site role.