Top Biotech Jobs in Denver & Boulder, CO

The Medical Science Liaison will support Tempus by educating healthcare professionals on oncology products and gathering insights for future developments, focusing on molecular oncology and genomic profiling.

As a Product Designer for Scientific Modalities, you will collaborate with teams to define product strategy, design and prototype solutions, and own design for initiatives.

The role involves developing customer-facing reports, providing insights, managing analytics for health systems, and collaborating cross-functionally to enhance operational efficiency.

The Senior Product Manager, Retention will enhance customer engagement and retention by leveraging data and cross-functional collaboration to optimize user experiences and lifecycle messaging.

The Chief Operating Officer will lead operational execution and manage delivery teams, drive company-wide operating rhythms, and partner closely with the CEO and leadership team to scale the organization and enhance operational effectiveness.

The role involves monitoring clinical trials, ensuring protocol adherence, managing data integrity, and training new employees, with significant travel required.

Lead and support clinical trials as a CRA II, ensuring compliance, monitoring sites, and managing data integrity with a focus on ophthalmology studies.

The Senior Clinical Research Associate will manage site monitoring, ensure compliance with protocols, assist with training, and report adverse events.

The Senior Clinical Informatics Sales Specialist drives adoption of informatics products by providing technical expertise, engaging with healthcare leaders, and developing sales strategies for genomic data analytics.

The Sr. Staff Product Marketing Manager will drive adoption of genomic platforms through competitive analysis, market research, and messaging development, collaborating across teams to inform positioning strategy.

The Senior Informatics Sales Specialist drives sales growth by providing subject matter expertise in genomics and informatics, consulting with customers on technical requirements, and collaborating with sales teams to enhance the customer experience. Responsibilities include customer presentations, technical guidance, and maintaining strong customer relationships.

The Lead Clinical Research Associate oversees clinical trial sites, ensuring compliance with regulations and protocols while mentoring CRAs and collaborating with teams to execute trials effectively.

As a Clinical Site Associate, you will support clinical trial operations including site compliance, documentation management, and collaboration with Clinical Research Associates.

The Senior Clinical Research Associate will oversee clinical trials, ensuring compliance, maintaining data integrity, and preparing study documentation while collaborating with investigators and site staff.

The Veeva RIM Administrator - Manager will oversee regulatory systems, document requirements, support validation teams, and educate users on system processes.

The Project Manager will coordinate customer relationships and manage global diagnostic initiatives, ensuring program success and compliance with regulatory standards.