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The Sr. Manager, Global Regulatory Affairs supports regulatory strategy, oversees submissions, manages queries, and collaborates with internal teams and CROs on compliance and implementation.

The Payment Specialist manages investigator payments, ensuring compliance with clinical trial agreements, resolving payment issues, and collaborating with various teams to support clinical trials effectively.

The Associate Director will provide regulatory strategic advice for U.S. communications, ensuring compliance with FDA regulations while collaborating with cross-functional teams to support materials for healthcare providers, payors, and patients.

The Sr. Manager, Clinical Trial Lead oversees clinical studies by developing operational strategies, collaborating with cross-functional teams, and managing CRO performance to ensure successful trial execution within budget and timelines.

The Clinical Trial Transparency Specialist manages clinical trial registration and results disclosure, liaises with vendors, and improves CTT processes, ensuring timely delivery and high quality of compliance.

The Senior Pharmacovigilance Lead manages safety operations, oversees PV resources, ensures compliance, and leads cross-functional safety governance in clinical programs.

Oversee clinical pharmacology plans for drug candidates, lead studies, analyze pharmacokinetic data, and engage with health authorities to guide drug development strategies.