Top Research Associate Jobs

As an Equity Research Associate, you will perform financial analysis, develop models, conduct in-depth research, and produce impactful reports while collaborating with a Senior Analyst.

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 Senior Research Associate supports research in cellular rejuvenation by executing laboratory experiments, developing techniques, and training others while contributing results to multiple projects.

The Clinical Research Associate will design and analyze clinical trials, ensuring protocol compliance, data integrity, and patient safety while collaborating with site staff and investigators.

The Clinical Research Associate II is responsible for overseeing clinical trials, ensuring compliance, training site staff, and managing site relationships while leveraging advanced capabilities for optimal study performance.

The role involves executing high-throughput plant transformation protocols, optimizing laboratory processes, documenting plant development, and collaborating with cross-functional teams in agricultural research.

The Research Associate I executes operational and testing activities at research sites, supports field trials, ensures accurate data collection, and supervises seasonal staff while adhering to safety standards.

The Research Associate will support a longitudinal clinical trial, recruit participants, conduct sessions, manage data, train assistants, and assist in lab operations.

The Equity Research Associate will support senior analysts in producing institutional-quality research, develop financial models, and participate in client interactions.

The Associate Director will lead research strategy, manage teams, create collateral, and deliver insights for Beauty, Style, & Entertainment verticals.

The Associate Manager will lead primary research projects, manage research panels, foster partnerships with stakeholders, and innovate methodologies to enhance research quality and engagement.

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

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

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

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.

The Clinical Research Associate is responsible for site management, ensuring protocol compliance, monitoring patient safety, and facilitating communication between the sponsor and investigational sites.

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

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

The Senior Clinical Research Associate will monitor cardiovascular devices, ensuring compliance with FDA regulations and managing study communication, while travelling regionally up to 65%.

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

Oversee and monitor clinical trial sites to ensure protocol, regulatory and GCP compliance; conduct site visits; manage multiple sites; ensure data integrity and participant safety; train and support site staff; collaborate with cross-functional teams and maintain stakeholder relationships.

The Clinical Research Associate will conduct site visits, ensure protocol compliance, review data, and collaborate with investigators to facilitate clinical trials.

As a Senior Clinical Research Associate, you will manage clinical trials, ensuring protocol compliance, data integrity, and patient safety, while collaborating with site staff and preparing study documentation.

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

The Senior Research Associate will execute molecular cloning and protein purification, maintain rigorous records, and collaborate with cross-functional teams to support therapeutic discovery operations.