Top Research Associate Jobs

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

As a Clinical Research Associate, you will conduct site visits for clinical trials, ensure compliance, and analyze clinical data. Collaborate with investigators, maintain data integrity, and contribute to study documentation.

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

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

The Senior Clinical Research Associate will oversee clinical trial activities, ensuring adherence to protocols, conduct site visits, and manage data integrity while providing support and training to site staff.

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 Sr. Clinical Research Associate manages sites for clinical trials, ensuring compliance with protocols and regulations, conducting monitoring visits, and collaborating with study teams.

The Lead Clinical Research Associate oversees clinical trial sites, ensuring compliance with regulations and protocols while mentoring CRAs and collaborating with teams to execute trials effectively.

As a Clinical Research Associate at ICON, you will design and analyze clinical trials, ensure protocol compliance, and collaborate with site staff for effective study conduct.

As a Clinical Research Associate, you'll oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements, managing sites, and supporting data integrity and participant safety.

Lead Clinical Research Associate will oversee and manage clinical trial sites, ensuring adherence to protocols and regulations while mentoring junior staff and ensuring data integrity.

The Senior Clinical Research Associate oversees site management and monitoring for clinical trials, ensuring compliance with GCP, patient safety, and quality execution of studies. Responsibilities include managing operational aspects, training site personnel, addressing protocol issues, and conducting monitoring activities.

The Senior Clinical Research Associate manages site monitoring to ensure data quality and compliance with clinical study protocols, while training junior CRAs and collaborating with study teams.

The Sr. Clinical Research Associate is responsible for site management and monitoring of clinical trials to ensure patient safety and compliance with regulations.

The Research Associate will support research for the HealthySteps program, assist in evidence management, provide technical assistance, and synthesize pediatric primary care literature.

The Senior Clinical Research Associate will oversee clinical study sites, ensuring compliance with regulations, quality of data, and patient safety while mentoring junior staff and supporting study management activities.

The Research Associate will support jury consulting research, analyzing data, conducting research on jurors, and collaborating with the team on projects related to trial strategy.

The Associate Director, Research Growth Strategy will lead product strategy and innovation for higher education, support product development, and manage a research team.