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The Third Party Quality Lead manages third-party quality risks in clinical operations, ensures GCP compliance, and oversees vendor performance and quality systems.

The Site Contracts Specialist reviews and negotiates clinical trial contracts, manages deliverables, and collaborates with cross-functional teams to address contract issues and compliance.

As a Global Contract Analyst, you will manage contractual agreements, ensure compliance with regulations, analyze contract terms, and guide project teams.

As a Senior CRA, you will manage early-phase oncology clinical trial activities ensuring compliance with protocols and regulatory standards, conducting site visits, training staff, and collaborating with teams for data accuracy.

The Clinical Research Associate will design and analyze clinical trials, ensuring protocol compliance, data integrity, and patient safety while collaborating with site staff and investigators.

The Quality ICM Issue Lead oversees quality event case management, leading investigations, notifications, root cause analysis, and process improvements within clinical development.

As a Senior Clinical Research Associate, you will oversee clinical trial processes, ensuring protocol compliance, data integrity, and patient safety while collaborating with site personnel and contributing to study documentation.

As the Manager of Feasibility, you will evaluate clinical trial feasibility, assess site capabilities, and develop recruitment strategies, ensuring successful study setups.

The Clinical Research Associate conducts site visits, ensures compliance with regulations, monitors patient safety, and aids in subject recruitment and data management.

Oversee cardiovascular clinical trials, ensuring compliance with regulations while managing site relationships and communication. Requires 3 years of monitoring experience and strong problem-solving skills.