Top Biotech Jobs in Denver & Boulder, CO

Lead cybersecurity requirements for the Digital Health Application (DiGA), including regulatory compliance and vulnerability management tasks.

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 Regional Sales Manager will lead sales activities, develop business plans, and manage key customer relationships in the MidAtlantic region, requiring frequent travel.

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 Product Manager for Chemistry will define and execute product vision, collaborate with teams to enhance small molecule R&D solutions, and leverage AI to improve scientific productivity.

Hands-on R&D internship supporting mechanical and electromechanical design, prototype assembly, fluidics/optics integration, testing (mechanical, thermal, fluidic), data analysis, and engineering documentation for life‑science instruments.

The Global EHS Manager leads and implements EHS programs, ensuring compliance and reducing incidents in global operations through collaboration and operational excellence.

The Senior Business Development Representative will qualify leads, build a pipeline for sales, engage with prospects, and collaborate with marketing to drive growth in life sciences SaaS.

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.

Provide field-based pre- and post-sales technical applications support for digital pathology and imaging systems: demos, proof-of-concepts, troubleshooting, training, workflow optimization, and scientific consultation to enable sales and ensure customer success.

Lead a global engineering organization to define strategy, drive hardware and systems product innovation, ensure regulatory compliance (ISO 13485), oversee end-to-end development, and partner cross-functionally to deliver scalable life-science solutions.

Lead and optimize US Market Access field inquiry programs and operational processes. Coordinate cross-functional teams and vendors, build dashboards, drive process improvements, support compliance (FUSE/MLR), and train stakeholders to increase execution effectiveness for product access.

Provide clinical and technical support for surgical imaging solutions across the UK. Deliver in-person and remote training, demonstrations, and theatre-based clinical support. Build relationships with clinicians and KOLs, run workshops and events, report market insights, and collaborate internally to drive adoption and growth.

Own and drive CT product-line sales strategy for Central and Southern Florida. Meet quarterly and annual revenue and order targets, grow market share, cultivate stakeholder relationships, lead cross-functional commercial teams, develop sales proposals aligned to customer budgets, and track activity using Salesforce.com to prioritize the sales funnel.

Own and execute the CT product-line sales strategy for Central/South Texas. Build relationships with hospitals, practices, and imaging centers, lead cross-functional teams to close deals, drive funnel growth, manage installed-base proposals, and meet quarterly and annual revenue and order targets while maximizing profitability.

The Manager, Site Resourcing will oversee site management for clinical research, coordinate teams and budget, and ensure compliance with regulations.

Manage end-to-end contract lifecycle for clinical trial operations: draft, review, negotiate agreements, ensure regulatory compliance, advise project teams, monitor contract performance, and maintain contract records.

The Clinical Research Associate will manage site interactions, conduct monitoring visits, ensure compliance, support recruitment, and oversee data management in oncology studies.