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The Regulatory Affairs CMC Intern supports regulatory projects by maintaining CMC information, preparing regulatory documents, and improving processes while gaining Biotech experience.

The Associate Director will operationalize and lead BeOne's clinical trial diversity strategy through data-driven insights and collaborations across Clinical Operations, enhancing patient enrollment diversity.

The Associate Director will lead the development of regulatory strategies, manage CMC submissions, and ensure compliance with health authority requirements for small molecules.

Manage regional study delivery, oversee clinical operations, ensure compliance and inspection readiness, and collaborate with stakeholders to meet study goals.

The Associate Director of Digital Clinical Operations enhances productivity in clinical trials through optimization of clinical systems, stakeholder engagement, requirement gathering, project coordination, and technology implementation.

The Associate Director leads and mentors clinical study managers, ensuring alignment with organizational goals and quality standards while managing study performance and resources.

The Senior Learning Business Partner will lead the GCO learning and development strategy, design training materials, and collaborate with stakeholders to meet global learning needs in clinical operations.

The Associate Director of Digital Clinical Operations enhances clinical trial productivity by managing CTMS applications, coordinating with stakeholders, and driving technology solutions to optimize clinical processes.

The Senior Clinical Research Associate manages site monitoring to ensure data quality and compliance with clinical study protocols, while training junior CRAs and collaborating with study teams.

The Head of Global Clinical Process Management oversees clinical operations processes, enhances efficiency, and collaborates cross-functionally to implement process improvements in global trials, particularly in oncology.