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As a Senior Regulatory Affairs Associate, you will manage regulatory processes, ensure compliance, and support product launches by collaborating with cross-functional teams and local health authorities.

The Senior/Vice President, Technical will lead regulatory strategy initiatives, advise clients on product lifecycles, and represent Parexel as an industry thought leader while mentoring colleagues.

Manage end-to-end labeling operations across global markets, ensure compliance with regulatory requirements, coordinate teams, and oversee drug safety activities.

The General Manager oversees FSP programs, ensuring high-quality service delivery, financial management, account growth, and operational excellence, while maintaining customer relationships.

The Senior Regulatory Affairs Consultant will ensure compliance of promotional materials with US regulations, support product launches, and provide regulatory guidance across teams.

The Principal Biostatistician independently manages complex clinical trials, providing statistical support and leading studies with regulatory impact while contributing to business development and client interactions.

The Sr. Clinical Research Associate is responsible for site management and monitoring of clinical trials to ensure patient safety and compliance with regulations.

Lead execution of complex publication programs in medical communications, manage projects, budgets, timelines, and collaborate with teams to ensure successful delivery.

Lead the data management team in clinical trials and medical affairs, ensuring quality data, project oversight, stakeholder engagement, and compliance with standards.