Top Research Associate Jobs

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 Equity Research Associate conducts analyses in the Life Insurance sector, develops financial models, and communicates findings to clients and stakeholders.

The Equity Research Associate will conduct fundamental analysis in the Auto & Auto Parts sector, provide research content, and communicate findings to clients.

The Principal Associate will lead research operations by optimizing processes, ensuring research governance, managing projects, and advocating for research best practices across the organization.

As an Associate Consultant, you'll enhance drug discovery using advanced analytics and research technology, collaborating with clients and interdisciplinary teams to deliver effective solutions and drive innovation.

The Associate will provide analytical support in structured finance, working with collateral performance and cash flow analysis while collaborating with investment banks and rating agencies.

The Systems Researcher focuses on algorithm development and software engineering, collaborating with computer scientists and data scientists in quantitative equity investment.

The role involves developing and applying statistical models, guiding market research strategies, and creating custom analyses for pharmaceutical clients while synthesizing results and maintaining client relationships.

The Senior Clinical Research Associate will manage clinical trials by conducting site visits, ensuring compliance, and contributing to study documentation.

The Post Doc Research Associate will work on advanced technology solutions in networking and distributed systems, contributing to research in areas like cloud computing and AI, supporting innovations in hybrid IT and IoT.

As an LCMS Research Associate III, you will manage samples, perform assays, maintain equipment, review data, and provide training in a laboratory setting.

Support customer insights and behavioral science projects: conduct qualitative and quantitative research, recruit participants, design surveys/interview guides, field surveys/interviews, produce data summaries, manage timelines and budgets, and collaborate cross-functionally.

Support product development for ELISpot and ELISA immunoassays by conducting experiments, troubleshooting assays, and collaborating with manufacturing teams.

The Research Associate I will develop monoclonal antibodies using hybridoma technology, including tasks like rodent immunization and immunoassay screening.

Perform site monitoring and management for clinical studies, ensuring compliance with protocols, regulations and quality standards. Collaborate with sites and manage project documentation and progress.

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

As a Clinical Research Associate, you will act as the liaison between investigational sites and sponsors, handle site visits, ensure compliance, monitor patient safety, and support site staff training and recruitment.

Oversee site relationships and perform selection, initiation, routine monitoring, and close-out visits for oncology trials. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety and drug accountability, support recruitment and data quality, escalate risks, and coordinate site payments and cross-functional partners. Travel up to 50% across the region.

The Senior Clinical Research Associate monitors clinical trials, ensures compliance with guidelines, supports studies, mentors junior staff, and maintains audit readiness.

The Clinical Research Associate will monitor oncology clinical trials, ensure compliance with regulations, support site training, and maintain documentation.

The Senior Clinical Research Associate will oversee 4-5 studies related to surgical devices, ensuring compliance with regulations and managing effective communication with stakeholders.

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 selection, initiation, monitoring, and close-out visits for oncology clinical trials; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor safety reporting, drug accountability, recruitment, data quality, and escalate issues while collaborating with cross-functional clinical teams.

As a Clinical Research Associate, you will conduct clinical trial monitoring, ensure protocol compliance, analyze data, and collaborate with site staff.

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