Top Research Associate Jobs

The Research Associate will perform experiments in immuno-oncology, utilizing mRNA technology for cancer therapy research, focusing on in vitro and in vivo studies, while collaborating with a team.

The Clinical Research Associate builds relationships with trial sites, ensures compliance with regulations, manages study oversight, and supports project delivery and documentation processes.

The Research Associate I performs procedures on laboratory animals, collects data, operates lab equipment, and supports study supervisors while ensuring compliance with protocols and GLP standards.

The Digital Research Associate conducts digital and social media analysis, synthesizing data for client strategies using AI tools and collaborating with internal teams.

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.

As a Senior Clinical Research Associate, you will act as the primary liaison between investigational sites and the sponsor, conducting site visits, ensuring compliance, monitoring patient safety, and assisting in recruitment efforts.

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

The Senior CRA will oversee clinical trial activities, ensure compliance with regulations, provide site support, and manage multiple projects. Requires experience in ophthalmology monitoring and high travel availability.

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

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.

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 conduct and monitor clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with site staff and investigators.

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.