Top Research Associate Jobs

As a Senior Clinical Research Associate, you will oversee clinical trials, ensuring adherence to protocols and regulatory standards, managing multiple sites, and collaborating with teams for data integrity and compliance.

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.

The role involves coordinating start-up processes for clinical trials, ensuring compliance, and maintaining documentation while collaborating with site personnel and operations teams.

The Senior Clinical Research Associate will oversee clinical trials, ensuring compliance, maintaining data integrity, and preparing study documentation while collaborating with investigators and site staff.

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

The Clinical Research Associate will conduct monitoring visits for clinical trials, ensuring compliance and data integrity, and preparing study documentation.

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 conduct clinical trial monitoring, ensure protocol compliance, analyze data, and collaborate with site staff.

The Senior Clinical Research Associate will monitor orthopedic studies, ensuring compliance with FDA regulations, managing risks, and maintaining relationships with stakeholders, while traveling frequently across the Western US.

The Clinical Research Associate will conduct site visits, ensure compliance and patient safety, and review clinical data with a focus on trial operations.

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.

Conduct complex research projects, design methodologies, analyze data, and supervise staff while ensuring compliance with regulations and reporting progress.

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 Senior Research Associate will support investment strategy research, analyze economic data, create financial models, and communicate insights to clients.

The Postdoctoral Research Associate will conduct experimental research on diffusiophoresis in microfluidics, analyze particle dynamics, and develop manipulation methods in complex geometries. The role includes supervising students and maintaining the lab, with a strong emphasis on publishing research.

Monitor clinical trial sites for compliance, provide support, manage data integrity, train staff, and ensure successful trial execution.

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

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.

As a Senior Clinical Research Associate at ICON, you will oversee clinical trial activities, ensuring adherence to protocols and regulatory standards while promoting data integrity and participant safety.

The Clinical Research Associate will conduct site visits for clinical trials, ensuring compliance, data integrity, and safety while collaborating with site staff.

The Senior Clinical Research Associate oversees clinical trial activities, ensuring adherence to protocols and regulations while managing data integrity and participant safety throughout the study lifecycle.

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 will manage clinical trial activities, ensuring compliance with protocols and regulatory requirements while training site staff and maintaining data integrity.

Oversee clinical trial activities, ensure compliance with protocols and regulatory requirements, and manage site performance. Provide training and support to site staff.

The Senior Clinical Research Associate oversees clinical trial activities ensuring compliance with protocols and regulations, manages site performance, and trains staff.