Top Research Associate Jobs

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.

As a Clinical Research Associate, you'll lead monitoring and compliance for clinical trials, ensure data integrity, and collaborate across teams.

As an Equity Research Associate, you will conduct industry analysis, build financial models, perform valuations, and communicate with clients, while demonstrating a strong interest in Specialty & Consumer Finance.

The Associate Director manages external research collaborations for Pfizer Oncology, oversees project execution, financial tracking, and drives continuous improvement in research processes.

As a Program Research Associate, you will verify program data and research new resources for a social care platform to help people in need. Your role involves data maintenance, responding to user requests, and collaborating in a team environment, all while ensuring the accuracy and inclusion of social services listed.

Conduct end-to-end AI and ML research, collaborate with teams, produce high-impact applications, and engage in the research lifecycle to advance cutting-edge AI research.

The role involves conducting market research, developing client solutions, and managing project plans while mentoring associates and communicating insights clearly.

The Clinical Research Associate will conduct clinical trial visits, ensure protocol compliance, analyze data, and prepare study documentation while collaborating with site staff.

Oversee and manage clinical trial activities, ensuring adherence to protocols, regulatory requirements, data integrity, and participant safety. Conduct site visits, provide support, and maintain relationships with stakeholders.

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.

The Clinical Research Associate will manage site interactions, ensure compliance, monitor trials, track data, and facilitate training and recruitment for oncology studies.

The Clinical Research Associate will design and analyze clinical trials, ensure protocol compliance, and maintain data integrity during studies.

As a Clinical Research Associate, you will monitor clinical trials, ensure protocol compliance, and collaborate with investigators while analyzing medical data.

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.

The role involves conducting clinical trial visits, ensuring compliance and data integrity, collaborating with site staff, and reviewing study documentation.

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 Clinical Research Associate will monitor clinical sites for adherence to protocols, ensure data integrity, manage communications, and oversee regulatory compliance throughout clinical trials.

The Clinical Research Associate 2 monitors clinical trials, ensures compliance with regulations, supports site management, and tracks study progress and documentation.

The Clinical Research Associate II will monitor clinical trials, manage sites, ensure patient safety, and verify data integrity for Phase I studies.

As a Clinical Research Associate, you will conduct clinical trial visits, ensure protocol compliance, and collaborate with site staff while maintaining data integrity and patient safety.

The Senior Clinical Research Associate will oversee clinical trial activities, ensuring compliance with protocols and regulatory standards while managing multiple projects and sites.

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 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.

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

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.