Top Research Associate Jobs

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

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.

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.

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.

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.

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

Support senior analysts covering Technology & Communications by building and maintaining financial models, conducting valuation and industry analysis, writing research reports and earnings previews, monitoring market and company developments, participating in calls and conferences, and preparing client presentation materials while developing deeper sector expertise.

Senior finance leader overseeing pre- and post-award research administration, grants management, compliance, internal controls, team leadership, process improvement, and partnership with central research offices to support sponsored and non-sponsored funding.

Support senior analyst covering Biotech by producing research publications, building and maintaining financial models, coordinating investor events, advising clients, and mentoring junior team members. Deliver clear, compliance-minded investment insights that inform global equity investors.

Lead ad sales research strategy and cross‑platform measurement for FOX, transforming multi‑platform data into client-facing insights, supporting pre‑sales, pitches, vendor relationships, dashboards, and mentoring junior researchers.

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

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.

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.

Perform molecular biology and mammalian cell culture experiments (cloning, PCR/qPCR, transfections, NGS prep), run microscopy and flow cytometry assays, analyze and present data, maintain detailed lab records, assist lab management and resource ordering, and contribute to project design and troubleshooting with mentorship; intended as a two-year stepping stone toward PhD preparation.

Serve as primary contact between investigational sites and sponsor. Conduct site selection, initiation, routine monitoring, and close-out visits. Ensure ICH-GCP and regulatory compliance, maintain CTMS and eTMF documentation, monitor patient safety and AE/SAE reporting, support recruitment and drug accountability, resolve data queries, track site budgets/payments, escalate risks, and collaborate with cross-functional clinical teams. Regional travel up to 50% required.

Manage site identification, qualification, and activation for cross-therapeutic clinical trials with a start-up focus. Conduct SQVs, coordinate regulatory and contract documents, drive site onboarding to Green Light, monitor KPIs and timelines, support inspections, and act as primary contact between sites, study teams, and stakeholders.

Run and support usability and learning studies with children and families: facilitate sessions, capture video/behavioral data, maintain lab equipment and scheduling, transcribe and code qualitative data, assist basic quantitative cleaning and analysis, and synthesize findings into presentation materials while upholding child safety and research protocols.

Develop and run ecological numerical models and conduct ADCP, wave, and water-quality observations in the Maryland Coastal Bays. Operate FVCOM and CE-QUAL-ICM models, co-supervise graduate and undergraduate students, and perform related research duties for a grant-funded faculty position.

Performs laboratory experiments and routine assays, prepares and analyzes specimens/tissue cultures, operates and maintains lab equipment, collects and statistically analyzes data, follows research protocols and good research practices, and contributes to publications while developing technical expertise.

Support a Senior Analyst covering electronic components, consumer hardware, and digital media. Conduct company and thematic research, build and maintain integrated 3-statement financial models, manage proprietary data sets and valuation comps, initiate independent research projects under tight deadlines, and communicate clear, evidence-based investment opinions in written reports and internal collaboration.

The Research Associate II will conduct molecular experiments, perform screenings for neurodegenerative diseases, and collaborate on projects involving CRISPR technologies.

The Research Associate will perform lab tasks including cell culture, DNA handling, and data analysis, using automated systems to assist in experiments and report preparation.

WireScreen seeks a Research Associate to enrich data with insights about global supply chains and risk. Responsibilities include data collection, quality assurance, customer support, and document analysis, requiring fluency in English and Mandarin with 2+ years experience in investigations or related fields.

As a Clinical Research Associate II, you will monitor clinical trials, ensuring protocol compliance and data integrity, while collaborating with site staff and investigators.