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The role involves developing, reviewing, and maintaining clinical trial documents like informed consent forms, ensuring compliance with regulations and guidelines while communicating with stakeholders.

The Senior CRA I is responsible for site monitoring, management of clinical studies, compliance with regulations, and leading small projects. Duties include ensuring proper protocol adherence, managing study data integrity, conducting visits, and training junior staff.

Develop, review, and maintain clinical trial documents like informed consent forms while ensuring compliance with regulations and guidelines.

The Startup Specialist will drive site activation, manage regulatory submissions, oversee compliance, and mentor colleagues in clinical research.

As an IT/Digital Solutions Intern at Fortrea, you will support proposal management by testing tools like Salesforce, collaborate with teams, and contribute to process improvements while gaining hands-on experience in technology-driven healthcare.

Lead Statistical Programmer overseeing programming activities for clinical trials, ensuring quality and adherence to standards, while mentoring team members.

The CRA I or CRA II monitors clinical study sites, ensures compliance with protocols and regulations, manages data integrity, and conducts site management tasks. Key responsibilities include coordinating projects, overseeing SAE reporting, and training new employees. Fluency in English and Polish is required, along with a life science degree and 3.5 years of monitoring experience.

The CRA II will monitor clinical trials, manage investigational sites, verify clinical data, train site staff, and prepare reports.

The Global Feasibility Lead II is responsible for data analysis, site selection strategies, project management, and leading feasibility initiatives in global clinical trials. They support proposal development and contribute to process improvements while mentoring junior staff.

The Senior CRA will conduct national monitoring for various therapeutic areas, focusing on oncology and other specializations, while working with multiple protocols.