Top Biotech Jobs in Las Vegas, NV

The Site Engagement Lead will manage participant recruitment and retention strategies for clinical trials, collaborate with teams, and improve engagement through educational resources and relationships.

The Senior Thought Leader Liaison coordinates between therapeutic area experts and commercial strategies, influencing market perceptions and driving demand for products through engagement and education. Responsibilities include managing relationships, translating insights into strategies, and enhancing patient access to therapies.

The Sr. Director, Clinical Scientist leads clinical research for Multiple Sclerosis therapies, overseeing study execution, protocol development, and cross-functional collaboration in a biotech setting.

As a Senior Data Scientist, you will develop statistical models and machine learning algorithms to improve patient enrollment and trial management while ensuring compliance in a healthcare data environment.

The Clinical Applications Specialist drives clinical education and training for General Imaging Ultrasound, enhancing customer competency and satisfaction while collaborating closely with sales.

The role is responsible for conducting QA audits, supporting compliance in GMP and Pharmacovigilance, and guiding quality issue management.

Coordinate technical support for GE diagnostic imaging equipment, assist field technicians, and manage customer relationships while ensuring compliance and quality standards.

Serve as a trusted advisor for strategic clinical accounts, build Customer Success Plans, monitor KPIs and customer health, drive adoption, expansions, renewals, and advocate customer needs across product and services.

The Sales Operations Analyst manages CRM hygiene, supports deal processes, conducts reporting and analytics, and implements AI solutions to enhance sales workflows.

The Compliance Manager, Transparency ensures compliance with reporting regulations, manages data accuracy, supports audits, and collaborates across teams for effective compliance processes.

The Senior Clinical Trials Scientist is responsible for leading the scientific execution of Phase II-III clinical trials, contributing to study design, regulatory documentation, and mentoring junior staff.

The Senior Clinical Programmer will develop and maintain programming for clinical trial data, ensuring data quality and compliance, while collaborating with other stakeholders. Responsibilities include troubleshooting, documentation, and mentoring junior programmers.

The Senior Director, Business Development will drive Cytel’s Pharma client relationships, create strategic sales plans, and oversee client-focused initiatives to expand business growth.

The Principal Statistical Programmer will generate and validate datasets, oversee deliverables from CROs, and ensure compliance with standards for clinical trials in a pharmaceutical setting.