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Clinical Trial Liaisons provide scientific support to clinical trial sites, optimize patient recruitment strategies, and engage with stakeholders to achieve trial goals. They require strong communication skills and a doctoral degree.

The Senior CRA will oversee clinical trial activities, ensuring adherence to protocols and regulatory requirements while managing multiple sites and projects.

The Senior Clinical Research Associate oversees and monitors clinical trials, ensures compliance with regulations, coordinates site activities, and manages trial-related issues effectively.

The Clinical Research Associate will monitor sites for compliance, manage documentation, ensure patient safety, facilitate training, and oversee drug accountability in oncology trials.

The Clinical Research Coordinator Nurse coordinates clinical trial procedures, performs technical requirements, collects patient data, and ensures trial compliance.

The Senior Clinical Research Associate monitors clinical trials, ensures compliance with regulations, mentors junior staff, and maintains quality and integrity of studies.

Senior Site Monitor responsible for planning and conducting on-site and remote monitoring across Phase I-IV studies. Ensures site compliance with protocol, data quality, and participant safety, conducts source data verification, manages site communications, supports RBQM processes, and participates in audits and inspections.

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.

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.

Monitor clinical trial sites, ensure adherence to protocols, conduct site visits, train staff, and manage relationships for oncology trials.