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As a Senior CRA, you will monitor clinical trial sites, ensure compliance with regulations, manage site performance, and train staff to maintain trial standards.

The Senior Clinical Research Associate will oversee 4-5 studies related to surgical devices, ensuring compliance with regulations and managing effective communication with stakeholders.

As a Clinical Research Associate II, you will design and analyze clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with site staff.

As a Senior Clinical Research Associate, you will manage clinical trials, ensuring protocol compliance, data integrity, and patient safety, while collaborating with site staff and preparing study documentation.

The Senior CRA will monitor clinical trial sites for compliance, conduct site visits, train site staff, and manage relationships with stakeholders in ophthalmology.

As a Clinical Rater, you will conduct assessments and rating scales for study participants, ensuring data integrity and participant safety during clinical trials.

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.

The Manager, Production Operations oversees day-to-day production activities, ensuring efficiency, quality standards, and alignment with organizational goals while leading a team and collaborating across departments for process optimization.

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.

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