Top Research Associate Jobs

Support experiment design, data collection, statistical analysis, and reporting within the DMPK department. Collaborate with scientists, maintain lab notebooks, and prepare reports.

Oversee cardiovascular clinical trials, ensuring compliance with regulations while managing site relationships and communication. Requires 3 years of monitoring experience and strong problem-solving skills.

As a Clinical Research Associate, you will liaise with investigational sites, ensuring compliance, monitoring studies, maintaining documentation, and supporting recruitment efforts in oncology trials.

Oversee and monitor clinical trial sites to ensure protocol, regulatory and GCP compliance; conduct site visits; manage multiple sites; ensure data integrity and participant safety; train and support site staff; collaborate with cross-functional teams and maintain stakeholder relationships.

The Senior Clinical Research Associate manages monitoring for cardiovascular clinical trials, ensuring compliance with FDA regulations and guiding teams to resolve site issues effectively.

The Research Associate will support senior analysts in investment idea generation and monitoring, conduct due diligence, and develop financial models.

Lead the design and governance of Bose’s research program portfolio, translating long-horizon research into phased, measurable programs and platform-ready capabilities. Define program charters, milestones, and investment gates; prioritize portfolio investments; coordinate cross-franchise efforts; and drive transitions of validated research into deployable platform components while communicating portfolio status and strategy to executive leadership.

Conduct quantitative portfolio and private markets research, build climate-aware capital market assumptions and stochastic simulation frameworks, design asset allocation analytics, and deploy AI-enabled, agentic workflows and tools to scale research and support portfolio construction and client engagement.

The Research Associate will perform laboratory tasks in NGS and Genomics, including nucleic acid extraction, library preparation, and operation of NGS instruments.

As a Research Associate at Merge Labs, you will conduct experiments in molecular biology, protein biochemistry, cell biology, and neuroscience, while collaborating across disciplines to advance core biological research and build experimental capabilities.

Execute and design laboratory experiments supporting reagent and assay development, analyze data, prepare reports/presentations, maintain lab inventories and equipment, troubleshoot assays, and adhere to safety and BSL-2 protocols while collaborating with peers and supervisors.

The Postdoctoral Research Associate will design a wearable ultrasonic imager for monitoring uterine contractions during pregnancy, conducting simulations, experiments, and device characterization.

Manage site relationships and monitor clinical trial conduct to ensure participant safety and data integrity per ICH GCP, regulatory requirements, and sponsor/SOPs. Conduct site selection, initiation, monitoring and close-out (onsite or remote), support regulatory submissions, maintain TMF and clinical systems, drive recruitment, report visit findings, and assist project management for successful study execution.

The Inhouse Clinical Research Associate supports clinical team activities, manages study documentation, and ensures compliance with regulatory standards.

The Clinical Research Associate (CRA) manages site relationships, ensures trial compliance, supports recruitment, and verifies trial data. They maintain documentation and facilitate regulatory submissions while monitoring site performance.

The Senior Clinical Research Associate will manage clinical trial sites, ensure protocol compliance, data integrity, and oversee monitoring visits. Responsibilities include training site personnel, supporting patient recruitment, and ensuring inspection readiness.

Support bioprocess development through executing bench-scale bioreactor experiments, optimizing cell culture, conducting statistical analysis, and communicating findings.

Perform hands-on protein biochemistry and molecular biology experiments: design plasmids, amplify/purify nucleic acids, express/purify/characterize proteins, measure binding (SPR, ITC, KinExa), run cell culture and transfection, and report results to the scientific team.

The Research Associate will assist in developing, executing, and analyzing market research projects for Fortune 500 companies, while receiving mentorship in various research methodologies.

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

As a Clinical Research Associate, you will monitor clinical trials, ensuring adherence to protocols and regulations, conduct site visits, and train staff.

The Clinical Research Associate will conduct monitoring visits, ensure protocol compliance, collaborate with site staff, and maintain data integrity.

Support and improve high-throughput pre-clinical QC workflows for mRNA and LNP materials. Execute and troubleshoot analytical assays (capillary electrophoresis, LC-MS, HPLC/UPLC, RT-PCR), operate and maintain automated liquid handlers and instrumentation, analyze and document data, support deviations/investigations, and contribute to workflow automation and continuous improvement in a fast-paced research environment.

Coordinate and execute in vivo and ex vivo nonclinical studies (efficacy, PK/PD, safety) using murine xenograft and humanized models. Contribute to study design and timelines, collaborate with CROs, perform necropsies and tissue processing, run downstream assays (flow cytometry, qPCR/ddPCR, ELISA), maintain experimental records, troubleshoot technical challenges, and support program advancement.

Support clinical study start-up and site activation by coordinating regulatory submissions, informed consent customization, essential document collection, and site readiness. Manage multiple site start-up workflows, track approvals and metrics in CTMS/eTMF, communicate with sites and stakeholders, escalate risks, and ensure compliance with ICH/GCP, MDR, GDPR and company procedures.