Top Research Associate Jobs

As a Clinical Research Associate, you'll lead monitoring and compliance for clinical trials, ensure data integrity, and collaborate across teams.

Design and execute complex molecular biology experiments (nucleic acid extraction, PCR/qPCR, NGS library prep, hybrid capture), operate liquid-handling automation, perform basic data analysis (Excel, R, Python), document results in digital lab notebooks, troubleshoot assays, and communicate findings to cross-functional teams to support assay research and early cancer detection test development.

As a Program Research Associate, you will verify program data and research new resources for a social care platform to help people in need. Your role involves data maintenance, responding to user requests, and collaborating in a team environment, all while ensuring the accuracy and inclusion of social services listed.

The role involves conducting equity research in energy and industrial sectors, developing financial models, and reporting on market trends under the supervision of senior analysts.

Analyze investment grade companies by performing credit analysis, monitoring industry trends, and collaborating with trading professionals. Prepare reports and present findings.

The Associate Consultant will leverage data analytics and market research to develop solutions for clients' business challenges and support project management.

The role involves providing quantitative and analytical support in fixed income research, performing credit analysis, and developing investment frameworks for Investment Grade bonds.

The Clinical Research Associate manages clinical trial site activation by conducting site qualification visits, ensuring compliance with regulations, and collaborating with study teams and site staff to achieve study timelines.

Conduct site qualification, monitoring, and close-out visits for clinical trials while ensuring compliance and data integrity. Collaborate with investigators and prepare study documentation.

The Clinical Research Associate will manage site interactions, ensure compliance, monitor trials, track data, and facilitate training and recruitment for oncology studies.

The Clinical Research Associate conducts site visits, ensures compliance with regulations, monitors patient safety, and aids in subject recruitment and data management.

As a Clinical Research Associate, you will manage site visits, ensure compliance with regulations, and oversee patient safety and data quality in oncology trials.

The Clinical Research Associate will manage site interactions, ensure compliance with regulations, monitor patient safety, and track budgets while supporting recruitment efforts and data quality.

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

Perform monitoring and site management for clinical studies ensuring compliance with protocols and regulations, managing site communication, and supporting recruitment and data integrity.

The Equity Research Associate supports analysis of biotechnology companies, builds financial models, and communicates findings through reports and presentations to clients.

The Equity Research Associate provides comprehensive market analysis and research on companies and industries. Responsibilities include data modeling, forecasting, and report publication, along with market monitoring and client interaction.

The Equity Research Associate analyzes and publishes research on corporations, industries, and financial markets, providing valuation and forecasting models for clients.

Join the Primary Production Technologies Group to develop next-generation adsorption technologies. Responsibilities include experiment design, data analysis, and collaboration on industrial projects.

The Equity Research Associate conducts market research, analyzes data, prepares financial models, and publishes reports on individual corporations and industries.

The intern will assist in quantitative equity research, working on projects related to stock selection models, portfolio construction, and communication of findings to the team.

Manage clinical research sites, ensuring protocol adherence, monitoring activities, recruitment, training staff, and maintaining communication with study teams.

Perform monitoring and site management for clinical studies, ensuring compliance with protocols and guidelines, and managing site communications and progress.

As a Clinical Research Associate, you will conduct various trial visits, ensure protocol compliance, and collaborate with investigators to maintain data integrity and patient safety.

Oversee and manage clinical trial activities, ensuring compliance with protocols and regulations, while mentoring site staff and maintaining data integrity.