Top Research Associate Jobs

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.

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

Conduct field research including biological sampling, acoustic and satellite tagging, deployment/maintenance of acoustic arrays, and telemetry and fisheries data analysis. Perform data entry, management, and analysis; assist with reports and peer-reviewed publications. Participate in offshore/nearshore research cruises and support NOAA Fisheries research objectives.

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 exploratory R&D by designing and running mammalian cell culture experiments, developing/validating cell-based assays, characterizing antibodies (SDS-PAGE, ELISA, flow cytometry), creating SOPs and ISO-compliant documentation, troubleshooting processes, and collaborating with R&D, manufacturing, and QC to enable product development and tech transfers.

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.

The Senior Clinical Research Associate manages clinical trial sites, ensures adherence to regulations, oversees study conduct, and resolves issues while safeguarding patient safety.

The Senior Research Associate will develop clinical-grade assays using NGS technologies, design experiments, analyze data, and collaborate cross-functionally to optimize performance and support cancer diagnostics.

Support senior analysts with bottoms-up equity research in the energy sector: build and maintain company and industry models, draft research reports, analyze industry data and news, maintain marketing presentations, and communicate investment ideas to institutional and internal clients.

The Clinical Research Associate supports Veracyte's clinical research, overseeing lab operations, managing specimens, ensuring compliance, and collaborating cross-functionally to monitor study execution.

Support and coordinate neurobehavioral research projects: program experiments, collect and analyze behavioral, ERP, and fMRI data, maintain lab operations, assist with IRB, manuscript/grant tasks, and mentor undergraduate assistants.

The Research Associate III leads clinical trial activities, mentors junior associates, ensures data accuracy, and participates in recruitment and protocol development.

The Research Associate supports clinical trial operations by collecting and managing patient data, ensuring compliance with protocols, and assisting with recruitment and informed consent processes.

Perform bioanalytical method development and LC-MS/MS quantitation for in vitro and in vivo ADME/DMPK studies, including MetID with LC-QTOF, PK sample analysis, CRO project management, data reporting, and maintaining electronic lab notebooks to support drug discovery programs.

Support research on potato diseases and plant-pathogen-vector interactions through molecular diagnostics and functional genomics. Plan and develop protocols, design/construct experimental equipment, run laboratory and greenhouse experiments, collect and analyze data, develop protocols, and train and supervise undergraduate students in a collaborative research environment.

The Clinical Research Associate 1 supports clinical trials by assisting with protocol preparation, site evaluation, monitoring studies, and maintaining documentation.

The Clinical Research Associate 1 supports clinical trials by designing protocols, monitoring site adherence, and managing documentation.

Provide support for clinical trials, assist in protocol design, conduct monitoring, evaluate clinical sites, and maintain study documentation.

Assists the clinical study team in research trials, including protocol design, site evaluations, study monitoring, and report preparation.

The Sr. Clinical Research Associate will support clinical studies by preparing protocols, monitoring sites, maintaining documents, and ensuring regulatory compliance.

The Clinical Research Associate 1 assists in clinical trial operations, including protocol design, site evaluations, study monitoring, and documentation for regulatory submissions.

Support clinical research activities, design protocols, generate SOPs, monitor studies, and prepare reports under supervision. Requires attention to detail and communication skills.

The Clinical Research Associate II assists in clinical trials by participating in protocol design, site evaluation, monitoring, and preparing reports. Responsibilities include generating SOPs, managing documents, and ensuring regulatory compliance.

Assist in clinical trial support including protocol preparation, site evaluations, monitoring studies, and reporting for regulatory submissions.

Provide Clinical Research support for trials, assist in protocol design, site evaluations, study monitoring, and preparation of regulatory documents.