Top Research Associate Jobs

Support analytical technical development by operating and troubleshooting instrumentation (HPLC, plate readers, liquid handlers), preparing samples, executing and analyzing assays, performing peer data review, enabling high-throughput workflows, aiding method development, executing improvement projects, collaborating with process development, and maintaining accurate documentation.

Support the senior semiconductor equity research analyst by building and maintaining financial models, producing company and industry research reports, organizing industry data, and communicating findings to sales, trading, and clients. Require strong modeling, writing, analytical, and client-facing skills.

Manage and monitor oncology clinical trial sites throughout the study lifecycle, ensuring data integrity, subject safety, inspection readiness, and regulatory compliance. Conduct on-site and remote monitoring visits, support IRB/EC submissions, manage essential documents and TMF reconciliation, review KRIs, implement CAPAs, train site staff, support inspections, drive site activation and engagement, and mentor junior CRAs as needed.

The Senior Clinical Research Associate is responsible for site management and monitoring of clinical trials, ensuring compliance with regulations and quality standards, and enhancing investigator site relationships.

Serve as primary contact between sites and sponsor to conduct selection, initiation, monitoring, and close-out visits. Ensure ICH-GCP and SOP compliance, maintain CTMS/eTMF documentation, monitor patient safety and AE/SAE reporting, support recruitment/retention, oversee drug accountability, resolve data queries, escalate risks, and collaborate with cross-functional clinical teams. Travel up to 50% across the southeast region.

Support ophthalmology research by conducting laboratory experiments and routine assays, collecting and analyzing specimens and data, maintaining lab equipment, contributing to publications, staying current on methods and literature, and following research protocols and safety policies.

Performs routine laboratory experiments and assays, collects and analyzes specimens or tissue cultures, operates and maintains lab equipment, records and analyzes data/statistics, follows research protocols and good research practices, and contributes to publications and ongoing learning.

Conducts in vitro and in vivo laboratory experiments supporting NIH-funded therapeutic discovery. Performs molecular biology (cloning, PCR/RT-PCR, viral vectors), cell- and biochemical assays, immunostaining, fluorescence/confocal microscopy, high-content screening, data collection and statistical analysis. Maintains lab equipment, supplies, notebooks, SOPs, and participates in meetings and publications under PI supervision.

Design, generate, and validate engineered mammalian cell lines (reporter, knock-out/knock-in, overexpression) using CRISPR and integrating expression systems. Optimize transfection/transduction, clonal isolation, genotyping, and readouts (flow cytometry, PCR, sequencing, imaging). Support differentiation experiments and collaborate across teams to monitor and improve cell fate transitions.

Lead and perform molecular and cellular immunology research on pathogen–host interactions and liver disease using in vitro and mouse in vivo models. Design experiments, analyze data, author publications/presentations, maintain lab protocols, safety and animal procedures, and support quality control and lab operations.

Monitor and support Alzheimer clinical trials: verify source data, ensure GCP/ICH/FDA compliance, assist Medical Safety and Clinical Monitors, review monitor visit reports, upload monitoring documentation to eTMF, and ensure data quality and integrity.

Conduct primary and secondary equity research including industry diligence, channel checks, earnings and management calls. Build and update detailed financial operating and valuation models (DCF, comparables, precedent transactions, LBO, merger modeling). Identify catalysts and investment theses, write concise research reports, and support client engagement with buy-side firms. Coordinate with analysts, sales, trading, and compliance to ensure research integrity.

Support a senior analyst covering the Biotech sector by producing equity research (earnings notes, initiations, thematic reports), building and maintaining financial models and relative value frameworks, advising clients, coordinating investor events, mentoring junior staff, and ensuring compliance and reputational risk oversight to deliver actionable investment insights.

Conduct fundamental equity research on Software sector companies: produce earnings previews/recaps, initiation and thematic reports; build and maintain financial models and relative value frameworks; support client inquiries and coordinate investor events; collaborate with senior analysts and mentor junior staff while adhering to compliance standards.

Provide clinical research support for trials by assisting in protocol design, site evaluation, budget procurement, monitoring studies, and preparing reports.

Supports conduct of oncology clinical trials by recruiting and screening participants, coordinating study visits, obtaining informed consent, arranging tests/procedures, performing protocol-required clinical lab activities, maintaining study documentation, entering sponsor data, and ensuring compliance with Good Clinical Practice and ICH guidelines.

Lead operational strategy and execution for LEO’s national research portfolio, overseeing project lifecycle from design to dissemination. Manage and develop a Research Operations team, coordinate cross-functional and external partners, establish scalable systems and processes, guide portfolio decision-making, and ensure high-quality, efficient implementation of impact evaluations to drive policy and community impact.

Lead business execution for Americas Research, delivering reporting, automating Excel models, preparing executive presentations, tracking metrics and expenses, negotiating market data contracts, and driving cross-functional initiatives to improve research franchise performance.

Support donor prospecting by researching individuals, foundations, and corporations using screening tools and databases. Create timely prospect profiles and capacity ratings, perform daily and ad-hoc wealth screenings, track donor news, assist with prospect management data integrity, and support reporting to advance fundraising initiatives.

Responsible for supporting clinical trials by assisting in protocol design, site evaluations, budget procurement, study monitoring, and report preparation.

The Clinical Research Associate II assists with clinical trial design, site evaluation, study monitoring, and regulatory compliance under supervision.

Assist in clinical research trials by supporting study teams, preparing documents, conducting site visits, and ensuring adherence to protocols.

Assist in the design, preparation, and monitoring of clinical trials, including protocol creation, site evaluation, and report generation.

Coordinate non-therapeutic pulmonary clinical research under PI/supervisor direction: screen, enroll, and recruit participants; schedule and monitor study activities; collect and enter data; recognize and report adverse events and protocol deviations; perform administrative and regulatory tasks including IRB submissions and protocol maintenance. May assist with higher-risk interventional studies. Some travel required.

Grant-funded, 12-month non‑tenure research faculty position to design and lead K‑12 education research and evaluation projects, pursue external funding, conduct quantitative and qualitative analyses, supervise staff and graduate assistants, disseminate findings, and represent the Center in collaborations.