Top Research Associate Jobs

Responsible for monitoring cardiovascular medical device studies, ensuring compliance with FDA regulations, and fostering effective relationships with stakeholders.

The Equity Research Associate will report to the Senior Analyst, develop research products, analyze the semiconductor industry, and communicate investment recommendations.

As a Clinical Research Associate, you will be responsible for site management, monitoring visits, training site staff, and ensuring compliance with regulations.

Monitor clinical trial sites to ensure compliance with protocols, manage regulatory submissions, and maintain communication with study teams and site staff.

Support lead analyst in U.S. High Yield Healthcare research, assist in credit investment ideas, financial modeling, and publication of reports.

The Senior Research Associate will perform quality control tests, manage data, support investigations, and assist in new product launches in compliance with quality standards.

Senior Site Monitor responsible for planning and conducting on-site and remote monitoring across Phase I-IV studies. Ensures site compliance with protocol, data quality, and participant safety, conducts source data verification, manages site communications, supports RBQM processes, and participates in audits and inspections.

This role involves supporting investment research analysts in assessing leveraged finance opportunities, performing due diligence, market research, and portfolio monitoring, while maintaining relationships with various teams within the business.

The Senior Clinical Research Associate will conduct site visits, ensure protocol compliance, collaborate with investigators, and maintain data integrity for clinical trials.

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

The role involves performing mammalian expression, establishing stable cell lines, characterizing molecules, and purifying proteins. The candidate must document work and present updates at meetings.

As a Senior Clinical Research Associate, you will monitor clinical trial sites, ensure compliance with protocols, and support site personnel in executing trials. Your role includes managing multiple sites, training staff, and upholding data integrity throughout the study lifecycle.

As a Senior Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements while managing site performance and collaborating with cross-functional teams.

The intern will assist with literature reviews, support research dissemination, develop project deliverables, and collaborate with team members.

Designs and executes antibody binding and immunoassay experiments (SPR/BLI, ELISA, FACS), analyzes data with GraphPad Prism, documents results in electronic notebooks, and collaborates to advance biotherapeutics programs. Supports protein expression/purification and other characterization tasks as needed.

The Research Associate will assist in private investment research, evaluate opportunities, maintain databases, manage deal processes, and support fund administration.

The role involves conducting molecular and cell biology experiments, performing mammalian cell culture, assisting in assay development, and collaborating in a research lab focused on genome editing and DNA repair.

The Research Associate will design and execute experiments in RNA therapeutics, manage RNA/cell cultures, and analyze data while maintaining documentation.

Coordinate and monitor clinical trials, maintain study documentation and status reports, manage queries and study cost efficiency, ensure regulatory compliance and patient safety, and build relationships with investigators and site staff.

As a Clinical Research Associate II, you'll conduct clinical trial visits, ensure protocol compliance and data integrity, and collaborate with site staff.

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

As a Clinical Research Associate, you will liaise with investigational sites, ensuring compliance, monitoring studies, maintaining documentation, and supporting recruitment efforts in oncology trials.

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

The Clinical Research Associate manages site contact for oncology studies, ensures compliance and safety, conducts monitoring, and supports recruitment and training efforts.