Top Research Associate Jobs

Coordinate and implement clinical study start-up and site recruitment for an Alzheimers diagnostic trial. Support site principal investigators and clinical staff, manage compliance, financial and personnel tasks, assist Clinical Operations with site recruitment, and communicate with sponsors. Full-time role with up to 20% US travel.

The position involves supporting research tasks, handling multiple responsibilities, and utilizing critical thinking to enhance processes. Excellent communication skills are essential for engaging with C-level executives.

Responsible for executing experiments and analyzing data in support of reagent and assay development. Involves general lab maintenance and preparation of reports.

The Research Associate executes experiments and analyzes data in support of biomarker measurement projects, maintains lab operations, and prepares reports under supervision.

This position executes experiments under supervision, analyzes data, prepares reports, and maintains lab equipment and supplies for biomarker research.

The Postdoctoral Research Associate will develop and evaluate health communication strategies to address disparities, manage research projects, and oversee students.

Perform on-site monitoring and site management to ensure protocol compliance, data integrity, and regulatory adherence. Conduct site selection, initiation, monitoring, and close-out visits; train sites; track recruitment, regulatory submissions, CRF completion, and TMF/ISF documentation; escalate quality issues and collaborate with study teams. May support start-up, recruitment planning, and site financial management.

The Postdoctoral Research Associate will work on multidisciplinary projects involving sustainable technologies and printed electronics, managing research activities and mentoring students, while contributing to publications and proposals.

The role involves conducting in vitro assays, analyzing samples, maintaining cell lines, and collaborating with a team on experimental design.

The Clinical Research Associate is responsible for site management, monitoring clinical studies, ensuring compliance with regulations, and supporting site staff in study-related matters.

Support asset class research and manager due diligence for public equities and fixed income: collect and analyze data from investment platforms, prepare reports and client materials, assist manager searches, organize meetings and minutes, maintain benchmarks and proprietary database, and serve as a resource for consultants and marketing.

Execute reproducible molecular biology protocols including cloning, transformations, PCR, protein expression and purification, and assay development. Operate and teleoperate robotic laboratory systems to generate demonstration data for autonomous experimentation. Collaborate with machine learning and robotics teams to identify failures, improve data quality, automate workflows, and expand protocol libraries. The role requires strong bench technique, precision, hand-eye coordination, and comfort with rapidly evolving laboratory technology.

Supports downstream protein purification, characterization, and process development for biopharmaceutical molecules. Performs chromatography, tangential flow filtration, viral clearance, filtration, analytical assays, and low-endotoxin production runs. Uses ÄKTA systems and biophysical instruments, analyzes and reports data, authors SOPs, supports tech transfer to GMP manufacturing, and contributes to process scale-up, scale-down, and timeline planning. The role is full-time onsite and may occasionally require work outside normal hours.

Conduct fundamental analysis, valuation, risk assessment, and financial modeling for biotechnology and pharmaceutical companies. Analyze scientific publications, clinical trial data, market news, and medical conference materials; interview executives and medical experts; write research reports for institutional clients and sales teams; answer client inquiries; and support senior equity research professionals with industry events and investment recommendations.

Executes and troubleshoots laboratory experiments supporting reagent, assay, and biomarker technology development. Analyzes experimental data using spreadsheets and graphing software, prepares reports and presentations, and communicates findings to review groups. Maintains laboratory supplies, equipment, inventories, and databases while following laboratory safety procedures, including BSL-2 practices. The role requires independent execution of complex experiments, strong scientific and analytical skills, and effective collaboration with limited supervision.

Executes and troubleshoots laboratory experiments supporting reagent and assay development, biomarker measurement, and technology research. Analyzes experimental data using spreadsheets and graphing software, prepares reports and presentations, and communicates findings. Maintains laboratory supplies, equipment, inventories, and databases, while following laboratory safety procedures including BSL-2 practices. The role requires independent execution of complex experiments, strong scientific and analytical skills, and collaboration across research and development activities.

Conduct and oversee clinical study site activities for Phase II–IV dermatology and rare disease trials. Responsibilities include site identification, initiation, monitoring, close-out, regulatory and ethics submissions, documentation, query management, feasibility assessments, cost efficiency, and potential CRA mentoring. Requires strong knowledge of ICH-GCP, medical data review, bilingual German and English communication, and willingness to travel internationally and domestically at least 60% of the time.

Conducts independent clinical trial site setup, monitoring, documentation, regulatory submissions, and close-out activities for Phase I–III studies in dermatology and rare diseases. Ensures ICH-GCP compliance, evaluates medical data, manages sponsor queries and study costs, and supports feasibility assessments. May train and mentor other CRAs. Requires substantial domestic and international travel, including driving.

Conducts independent clinical study start-up, monitoring, documentation, regulatory submissions, and site close-out for Phase II–IV dermatology and rare disease trials. Ensures compliance with ICH-GCP, evaluates medical data, manages sponsor queries and study costs, and may train fellow CRAs. Requires at least 18 months of CRA monitoring experience, a relevant college degree, German and English fluency, a valid driving license, and travel of at least 60%.

Support public health research and evaluation by collecting qualitative data (surveys, interviews, focus groups), coordinating grant development and submissions, assisting literature reviews and reporting, providing training/technical assistance to Tribal organizations, maintaining website content, and performing related administrative duties with occasional travel.

Perform quantitative and qualitative research on funds and investment vehicles, develop forward-looking ratings, author research reports, conduct manager interviews and on-site due diligence, monitor industry and market developments, and improve database accuracy and methodologies.

Advise senior executives on enterprise strategy and transformation. Design workplans, conduct research and stakeholder interviews, perform quantitative analysis, develop recommendations, craft executive storylines, and present findings. Contribute to recruiting, talent development, and team initiatives.

Conduct and design complex laboratory experiments supporting gene therapy projects. Execute bench work, analyze data, prepare technical reports and protocols, maintain GMP/GLP-compliant documentation, troubleshoot, and contribute as an expert team member or principal investigator.

The Crypto Research Associate will focus on conducting investment research in decentralized finance, developing frameworks for token evaluation, and collaborating on product development and thought leadership.

Support quantitative research, portfolio management, and risk teams by developing and maintaining quantitative models, portfolio construction and risk processes, addressing data and analysis requests, communicating results, and participating in research projects to enhance tools and models.