Top Research Associate Jobs

Provides strategic and hands-on biostatistical leadership across pharmaceutical discovery, translational, biomarker, and early research programs. Designs studies, analyzes complex biological datasets, develops advanced statistical methods and reproducible R workflows, and translates evidence into portfolio decisions. The role collaborates with quantitative and scientific functions, supports publications and external partnerships, mentors statisticians, and advances data-driven analytical practices.

The Associate Director will lead research strategy, manage teams, create collateral, and deliver insights for Beauty, Style, & Entertainment verticals.

Conduct fundamental research and financial modeling on public and private companies across emerging, frontier and developed markets. Screen debt and equity opportunities, monitor portfolio assets, manage private securities and restructurings, engage with management and industry experts, and travel to conferences and company visits to support the investment process alongside portfolio managers, analysts, and traders.

Monitor clinical trial sites including initiation, routine monitoring, and close-out. Ensure protocol adherence, informed consent, data integrity (CRFs/EDC), SAE reporting, registry management, feasibility, and coordinate local project activities. Provide training and liaise with vendors and clients; perform on-site and remote monitoring with significant travel.

Conduct research on bacterial diseases of tree fruits (e.g., fire blight), using microbiology, genome sequencing, comparative genomics, and bacterial genetics to develop controls and biopesticides. Work with growers and stakeholders, train students, maintain records, present findings, and publish manuscripts. Position includes in-state and regional travel.

Support FinTech equity coverage by building and maintaining financial models, conducting company and sector research, analyzing market and regulatory trends, authoring research reports and investment recommendations, and engaging with institutional clients and internal stakeholders to present findings and support investor outreach.

Perform onsite and remote clinical site monitoring (PSV, SIV, IMV, COV), ensure protocol and regulatory adherence, manage study documentation and audit readiness, mentor junior staff, support site selection and RFPs, and contribute to clinical operations and SOP development across multiple protocols with significant travel.

Postdoctoral researcher to develop, test, and document methods for production, separation, and purification of medical and research radioisotopes. Plan experiments, follow safety/operations procedures, prepare manuscripts and presentations, collaborate across teams, and contribute to proposal development within a 2-year term.

The Clinical Research Associate will monitor sites for Oncology studies, ensuring compliance with protocols and managing communications and documentation.

Execute established R&D laboratory protocols, perform experiments and basic data analysis, manage lab inventory and compliance, maintain safety culture, train team members, and support biosensor development under senior guidance.

Onsite bilingual (English/Mandarin) research associate supporting Phase I clinical trials: recruit and screen participants, conduct protocol visits, maintain study logs and supplies, handle samples, assist physicians and monitors, ensure participant safety and data quality, and follow clinical operating and quality management guidelines.

Join an equity research team to analyze publicly traded companies, build and update financial models, gather proprietary market and industry data, develop industry relationships, attend events, produce written research reports, and support internal sales distribution.

Lead design, development, and optimization of electrochemical CMOS sensors and workflows. Develop acid-generation solutions from CMOS electrodes, run advanced electrochemical characterization, analyze data for sensor optimization, communicate results to stakeholders, and mentor junior scientists in cross-functional teams.

Support development and manufacture of reagents and consumables by authoring and executing SOPs, performing controlled experiments and equipment validation, investigating non-conformances, implementing process improvements, maintaining GMP/GDP documentation, training staff, and collaborating cross-functionally to meet quality and regulatory requirements.

Support development and GMP manufacture of reagents and consumables by authoring and executing SOPs, running controlled aseptic experiments, performing equipment validation, investigating non-conformances, proposing process improvements, maintaining documentation and compliance, training staff, and collaborating cross-functionally to meet project objectives.

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.

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

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.

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.

The Research Assistant/Associate will design experiments, collect and analyze data, and report findings in the ADME department, collaborating with in vitro biologists.

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

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

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

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