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As a Senior Statistical Programmer, you will develop and validate SAS programs for clinical trial data analyses, support regulatory submissions, and lead studies, impacting patient health globally.

Responsible for monitoring clinical sites, ensuring adherence to protocols, managing data integrity, conducting site management, and assisting in training and development of new employees.

Manage clinical study sites, perform monitoring duties, ensure compliance with regulations, safeguard data integrity, and prepare project plans for clinical monitoring.

Manage clinical studies, conduct site monitoring, ensure compliance with regulations, safeguard data integrity, and support study teams with project plans and training.

The Senior CRA is responsible for site monitoring, management, and compliance with regulatory guidelines for clinical studies. Duties include managing study sites, ensuring data integrity, and overseeing recruitment and adverse event reporting.

The Central Monitoring Specialist conducts central monitoring activities, collaborates with study teams, performs risk assessments, and manages project risk data to ensure study compliance and execution.

The Start-up Specialist oversees clinical trial start-up tasks, ensuring timely project execution while supervising team performance and maintaining client relationships.

Responsible for clinical site management and monitoring for clinical trials, ensuring adherence to protocols, regulatory requirements, and data integrity. Conduct site visits, prepare project plans, and collaborate with study teams while maintaining compliance and audit readiness.

This role involves developing and reviewing clinical trial documents, ensuring compliance with regulations and clarity for participants, and communicating with stakeholders.

Responsible for developing, reviewing, and maintaining informed consent forms for clinical trials, ensuring compliance with regulatory guidelines and effective communication with stakeholders.