Top Biotech Jobs in Denver & Boulder, CO

The Medical Science Liaison will educate healthcare providers on Tempus oncology products, support commercial objectives, and maintain KOL relationships.

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 Product Manager will define and execute the product strategy and roadmap for Benchling's small molecule R&D solution, collaborating with teams to deliver solutions for scientific research.

Responsible for scientific oversight and quality of clinical trials in Late-Stage Oncology, collaborating with teams and presenting data, while ensuring compliance and optimizing procedures.

As a Client Services Tech, you will coordinate sample-related activities, process and document data, and provide laboratory support training.

The Account Manager will focus on generating sales plans, educating clients about wound care products, and maintaining relationships with healthcare professionals.

The Senior CRA ensures quality execution at clinical trial sites, conducts oversight visits, supports compliance, and enhances quality performance across studies.

The Principal Manager, CQM leads document development and management, oversees compliance with procedures, and supports audits in clinical trials.

The Clinical Research Associate will conduct site visits for clinical trials, ensuring compliance, data integrity, and safety while collaborating with site staff.

The Hybrid Immunization Specialist drives healthcare provider engagement and vaccine uptake by educating on disease prevention and GSK's vaccine portfolio, collaborating closely with sales and account teams.

The Oncology Account Manager will drive sales and manage business activities in the designated territory, working collaboratively with cross-functional teams to enhance access to GSK therapies and engage key customers.

The Immunization Specialist educates healthcare providers on GSK's vaccine portfolio, drives vaccine uptake, and supports immunization goals through effective customer engagement.

The Process Validation Engineer is responsible for executing process validation activities in oligonucleotide API manufacturing, including design, execution, and reporting of validation studies and ensuring compliance with regulatory standards.

Responsible for managing technical product requirements for Learning Services platforms, translating customer needs into technical solutions, and collaborating with cross-functional teams to enhance product offerings.

The Manufacturing Representative will ensure on-time delivery of products, validate equipment, and resolve manufacturing issues in a GMP environment.

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

Oversee Quality Control data tracking and reporting, collaborate with QC teams, maintain tracking systems, ensure compliance, and coordinate QC activities.

This role involves site monitoring and management for clinical studies, ensuring compliance with regulations and overseeing project plans. Responsibilities include data integrity checks, training staff, managing little projects, and maintaining communication with stakeholders.