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Manage and coordinate clinical research studies, ensuring compliance with regulations, maintaining study documentation, and facilitating communication among stakeholders.

The role involves site qualification, monitoring, management, and compliance with clinical protocols, while ensuring patient safety and data integrity. Responsibilities include verifying informed consent, maintaining documentation, and managing investigational products at clinical sites.

Oversee cash application process, perform reconciliations, implement improvements, analyze reports, mentor junior staff, ensure compliance, assist with audits, and process customer refunds.

The Safety & PV Specialist assists in pharmacovigilance program delivery, including the processing of safety reports, data management, and adherence to regulatory guidelines.

The R Statistical Programmer develops programming code, ensures quality outputs, collaborates with teams, and manages multiple projects while adhering to regulatory guidelines.

Coordinate safety and pharmacovigilance activities, including data management, cleaning, validation, and adherence to regulatory guidelines.

The role assists with safety and pharmacovigilance tasks including data management, cleaning, validation, and adherence to regulatory guidelines.

The CRA performs monitoring, site management, and compliance tasks, ensuring adherence to regulations and supporting study site personnel in clinical trials.

The role involves supporting clinical operations by maintaining trial master files, ensuring compliance, and communicating with study teams, while managing multiple tasks effectively.

The Senior HRIS Analyst leads HRIS projects, provides global support for HRIS applications, ensures data integrity, and develops procedures and user guides while training HR staff on system functionality.