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

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 Clinical Research Associate will conduct monitoring visits for clinical trials, ensuring compliance and data integrity, and preparing study documentation.

As a Clinical Research Associate, you will conduct clinical trial monitoring, ensure protocol compliance, analyze data, and collaborate with site staff.

The Clinical Research Associate will conduct site visits, ensure compliance and patient safety, and review clinical data with a focus on trial operations.

The Clinical Research Associate will conduct site visits, ensure protocol compliance, and review clinical data for trials. Responsibilities include collaborating with investigators and preparing study documentation.

As a Clinical Research Associate, you'll conduct clinical trial visits, ensure protocol compliance, manage data quality, and assist in study documentation.

Conduct site qualification, monitoring, and close-out visits for clinical trials while ensuring compliance and data integrity. Collaborate with investigators and prepare study documentation.

The Scientific Affairs Specialist I supports scientific liaison activities for central laboratory services in clinical trials, ensuring scientific rigor and compliance. Responsibilities include managing test information, supporting assay selection, and collaborating with cross-functional teams.

Lead one or more Clinical Data Science project teams, oversee project initiation, planning, and execution, and manage communication with clients and vendors. Four key responsibilities include quality control, issue tracking, project kick-off facilitation, and support in sales efforts.