Top Tech Jobs & Startup Jobs in Denver & Boulder, CO

Support implementation of the Culture of Quality program, enhance Quality communications (webpage, newsletters, sessions), create a Quality department storyboard, produce graphic and digital content, collect and analyze data, and collaborate cross-functionally to advance quality initiatives.

Remote summer intern supporting the Employee Relations team: transcribe interviews, conduct pre-investigation research, draft documentation and summary reports, maintain Ethics Point case records, and assist ER data analysis and reporting.

Lead market and industry analysis, perform due diligence on strategic initiatives, build presentations for leadership and board meetings, maintain strategic databases, and collaborate across teams to develop actionable recommendations supporting company growth and innovation.

Support Privacy and Data Ethics counsel with legal research, policy and training drafting, contract and vendor reviews, privacy assessments, and project tracking to ensure compliance with global data protection laws (e.g., GDPR, HIPAA) across cross-functional teams.

Lead global strategic feasibility for clinical studies by integrating internal and external data, advising country/site selection, recruitment and operational strategies, improving feasibility processes and tools, and partnering with program and study teams to optimize study design and execution across early to late-stage programs.

Support modernization of onboarding by converting presentations into AI-generated avatar videos (e.g., Synthesia), drafting scripts, standardizing automated onboarding modules, analyzing feedback, exploring generative AI tools, and developing scalable templates for internal communications.

The Executive Director leads Global Clinical Pharmacology & Development Technology Solutions, overseeing technology strategy, solution delivery, and team leadership to support R&D initiatives in cancer treatment.

Lead the U.S. Biologics Regulatory CMC organization, develop global CMC regulatory strategies, oversee CMC submissions and health authority interactions, manage a ~15-person team, ensure compliance and inspection readiness, and support lifecycle management for biologics including mAbs, ADCs, cell therapies, and combination products.