Top Biotech Jobs in Denver & Boulder, CO

The Payer Engagement Account Director will drive payer opportunities, build relationships with payers, lead meetings, and collaborate cross-functionally to advance access to the company's cancer detection technology.

The Sales Director will lead the sales process to close partnerships with research sites, managing all sales activities including discovery and negotiation, while collaborating with Customer Success for onboarding.

The Senior Payroll Specialist oversees US payroll processing, supports EMEA payroll, ensures compliance, and drives cross-functional process improvement initiatives.

The Independent Vaccine Contract Manager collaborates with various stakeholders to ensure effective pricing and contracting discussions for Pfizer's vaccine portfolio and manages all contracting activities with assigned accounts in a compliant manner.

The role involves supporting commercial objectives by educating healthcare providers on Tempus oncology products through presentations and managing key relationships in oncology.

The Executive Director will lead early clinical development in neuroscience, oversee clinical trials, ensure regulatory compliance, and manage team collaboration and strategy for drug submission supporting both preclinical and clinical phases.

The Senior Director leads global pharmacovigilance operations, ensuring compliance, managing safety reporting, and collaborating across functions while overseeing vendor relationships and enhancing capabilities.

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.

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.

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 development and operationalization of LLM, agentic, and image AI solutions for diagnostics. Build multimodal datasets, implement RAG and agent workflows, apply ML and statistical methods (DoE, Bayesian optimization, causal/survival/longitudinal), analyze RWE/RWD, and integrate insights across clinical, regulatory, and product teams to drive diagnostic and business impact.

Lead global digital manufacturing and intelligent automation strategy, drive implementation of cloud, AI, IoT and analytics solutions, build capability center, manage cross-functional teams and vendor relationships, measure KPIs, ensure regulatory and data security compliance, and drive organizational change to adopt digital tools.

Responsible for conducting market research and product evaluations, guiding teams with insights, and communicating findings to stakeholders.

As a Manufacturing Representative, you will ensure on-time delivery, handle manufacturing of oligonucleotide APIs, validate new equipment, and solve quality issues in a GMP environment.

The Research Associate leads oligonucleotide project development including synthesis and purification, ensuring compliance with SOPs and cGMP, while documenting results and supporting technology transfers.