As a Clinical Research Associate, you will conduct clinical trial site visits, ensuring compliance and data integrity while collaborating with site staff. You will also prepare study documentation.

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 II, you will design and analyze clinical trials, ensure protocol compliance, and review clinical data while collaborating with site staff.

Conduct site qualification, monitoring, and close-out visits for clinical trials while ensuring compliance, integrity, and patient safety throughout the trial process.

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 role involves managing the grant application process, researching funding opportunities, collaborating with stakeholders, ensuring compliance, and tracking grant activities.

As a Central Review Coordinator, you will coordinate centralized review activities for clinical trials, ensuring data collection and compliance with regulatory standards.

The Senior Clinical Data Science Programmer develops and implements programming solutions for clinical trial data analysis, ensuring data accuracy and efficiency while collaborating with various teams.

Manage contractual agreements, ensure compliance, provide guidance on contract interpretation, and assist in contract management processes.

As a Clinical Research Associate II, you will manage clinical trials, ensuring compliance and data integrity while collaborating with site staff.

As a Senior CRA, you will manage clinical trial activities, ensuring data integrity and compliance while fostering relationships with trial sites and overseeing monitoring visits.

Design professional PowerPoint presentations for clinical research, collaborating with teams to ensure accuracy and branding while managing multiple projects under tight deadlines.

Lead and coordinate centralized review activities for clinical trials, ensuring accuracy and compliance with regulatory standards while providing team leadership.

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

As a Senior Clinical Research Associate, you will oversee clinical trial activities, ensuring adherence to protocols and regulatory requirements while managing relationships with site personnel and stakeholders.

The Senior Account Executive will develop client relationships, drive sales initiatives, manage the sales process, and enhance client satisfaction in the clinical development field.

The Manager, IT Operations oversees IT infrastructure management, drives process improvements, coordinates teams, and ensures operational efficiency while managing budgets and resources.

Oversee and manage clinical trial activities to ensure compliance with protocols, regulatory requirements, and industry standards. Conduct site assessments, monitor trials, and facilitate audits.

The Financial Analyst II will prepare financial reports, conduct financial reviews, partner with teams on financial health, and support month-end processes.