Top Research Associate Jobs

Build and manage a medical device sales territory across outpatient urology and urogynecology clinics. Prospect physicians and clinical staff, deliver product education and demonstrations, drive catheter and urinary management system prescriptions, maintain CRM pipeline data, and achieve activity and revenue targets. The role requires daily field travel, disciplined cold outreach, strong communication, quota achievement, and business ownership, with training provided on clinical topics and advancement opportunities to Territory Manager.

Develop and optimize upstream and downstream biologics manufacturing processes for early- to late-stage products. Responsibilities include designing and executing experiments, characterizing unit operations, integrating process control and monitoring platforms, conducting laboratory and pilot-scale studies, supporting scale-up and technology transfer, collaborating cross-functionally, and maintaining a safe, compliant laboratory environment.

Provides scientific and operational leadership for early-phase vaccine clinical trials, including study design, execution, safety assessment, data interpretation, risk management, regulatory compliance, and cross-functional team leadership. Authors clinical and regulatory documents, manages complex trial programs, develops procedures, mentors junior staff, supports submissions and investigator initiatives, and coordinates project planning, issue mitigation, governance, and stakeholder communications.

Supports Technology and Internet equity research by building earnings and valuation models, analyzing industry trends, producing written research publications, developing management and industry relationships, and communicating stock views and industry themes to institutional investors, trading desks, and internal stakeholders. The role requires strong quantitative, communication, teamwork, organizational, and Excel skills, along with an undergraduate degree in a relevant quantitative or finance-related field.

Conduct laboratory experiments, collect and analyze tissue and clinical data, maintain lab equipment and databases (SPSS, IBIS), perform quality control and statistical analyses, prepare neuropathology summaries and compliance reports, support tissue banking operations and donor record management, and collaborate with investigators to generate research datasets and reports for NIH-funded projects.

Develop, optimize, troubleshoot, and execute analytical assays to characterize transgene expression and function in genetically edited porcine cells. Perform primary cell isolation and mammalian cell culture, and run flow cytometry, ELISA, and PCR-based assays. Maintain reagent inventory, document data in ELNs, lead internal technology transfers with QC, conduct root-cause analyses for assay issues, and present findings to cross-functional teams in a fast-paced start-up environment.

Perform and manage laboratory research on DNA damage response, DNA repair, and nucleic acid–based therapeutics. Design and execute complex experiments using ASOs, siRNA, and miRNA; collect and analyze data; develop methods; prepare manuscripts and funding proposals; coordinate lab personnel and maintain equipment.

Lead site management and monitoring for oncology clinical trials, ensuring data integrity, subject safety, inspection readiness, and regulatory compliance. Perform on-site and remote monitoring, train and mentor CRAs, manage TMF/essential documents, drive site activation and engagement, and implement CAPA and KRI oversight.

Develop an AI-driven dual robotic system combining a vision-language planner with a fast reactive controller for precision fluid handling in radioisotope production. Build 3D perception for fluid-state estimation, develop reactive control methods, validate on a cold bench, collaborate across robotics, radiochemistry, and ML communities, and publish results in peer-reviewed venues.

Perform high-throughput molecular lab work including DNA isolation, fragmentation, PCR/qPCR/ddPCR, and NGS library preparation. Follow SOPs, use LIMS, operate automated liquid handlers, document results, maintain quality control, manage inventory, troubleshoot, and meet aggressive timelines in a startup environment.

Perform supervised R&D to develop reagents, materials, and processes for genomic manufacturing technologies. Conduct organic synthesis, analytical testing (LC, MS, HPLC, NMR, FTIR, UV, fluorescence), instrument calibration, documentation, SOP preparation, and support pilot manufacturing and QC operations.

Perform synthesis and analytical characterization of small molecules, nucleotides, and oligonucleotides; develop surface modification and bioconjugation chemistries; document and analyze experimental data; collaborate with and supervise technical staff to advance nucleic acid sequencing technologies.

Perform analytical testing and method qualification of biotherapeutic samples (HPLC, SDS-PAGE, SDS-CGE, ELISA, UV-Vis), execute protocols, analyze and document data, troubleshoot experiments, present findings, maintain lab safety, and collaborate with cross-functional teams and clients.

Support Senior Analyst on life insurance equity research by building and maintaining financial models, analyzing regulatory filings and industry trends, drafting research reports, responding to client and internal inquiries, and collaborating with global GIR teams to produce actionable investment insights.

Develop, optimize, and scale assay and reagent workflows for a diagnostics platform. Create robust protocols for reagent manufacturing, array fabrication, and assay execution. Support process characterization, QC, stability, and verification studies. Prepare reagents and maintain lab operations, collect and analyze data, troubleshoot experiments, and collaborate cross-functionally to implement improvements toward regulated product development.

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.

Part-time on-call Research Associate supporting federal communications: review and score client programs, join consensus calls, respond to quick-turn requests, produce and edit reports and presentations (Excel, PowerPoint, Word), coordinate with project leads and clients, and participate in special projects. Expect ~8 hours or less per month; must reside and work within the continental US.

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 Research Associate will conduct experiments using cellular immunology techniques, manage cell cultures, and perform data analysis. Strong organizational skills and independence are essential.

Support a human neurostimulation study by recruiting participants, coordinating and executing experiments, collecting and managing data, maintaining documentation, and assisting with analysis and reporting.

Assist in the development of automated workflows in cell and organoid culture, utilizing robotics and tissue engineering for biomedical research.

Conduct experimental research within the Yu Research Group: collect and analyze data, perform experiments, maintain lab equipment and supplies, assist manuscript and grant writing, and perform other assigned duties.

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.

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

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