Top Research Associate Jobs

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.

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.

As a Senior CRA / CRA II, you will manage and oversee clinical trial activities, ensuring compliance with protocols, regulations, and industry standards through monitoring and site visits.

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

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

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.

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 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.

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

The Senior Clinical Research Associate manages study sites, ensuring compliance with regulations and high performance. Responsibilities include site selection, monitoring, training site staff, and data management.

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

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 Associate Director will manage market research initiatives, providing insights to support brand decision-making and competitive intelligence in the pharmaceutical industry, while collaborating closely with the marketing team.

The Associate Director will manage market research to support brand decision-making, using primary and secondary research to inform strategies and track brand performance in the oncology sector.

The Associate Director will develop research agendas and design projects addressing strategic and operational issues in education, focusing on administrative effectiveness through data analysis and stakeholder collaboration.