Top Biotech Jobs in Huntsville, AL

The Principal Statistical Programmer manages statistical programming for clinical trial data, ensures quality and compliance for CDISC standards, and mentors junior staff.

The DevOps Engineer role focuses on integrating continuous delivery practices, maintaining CI/CD pipelines, collaborating with teams on infrastructure automation, and ensuring compliance standards.

Manage global clinical studies activities, support document development, site management, and compliance while guiding clinical sites and training staff.

The Senior CRA will oversee clinical trial activities, ensuring adherence to protocols and regulatory requirements while managing multiple sites and projects.

The Senior Clinical Research Associate will conduct site visits, ensure trial compliance, review data, and prepare study documentation.

The Associate Director, Global Congresses leads planning and execution of major oncology congresses, coordinating cross-functional teams and managing operations, budgets, and stakeholder communications.

The Associate Director, Platform Engineering is responsible for building and maintaining a digital platform, overseeing engineering strategy, compliance, team mentorship, and cross-functional collaboration to ensure platform reliability and innovation.

Lead the Central Statistical Monitoring team, ensuring subject safety and data integrity in clinical trials through statistical analysis and collaboration with various stakeholders.

The Lead Clinical Data Manager oversees all clinical trial data management processes, ensuring compliance, accuracy, and timely database management from study start to close, and collaborates with teams to resolve data issues while maintaining adherence to regulatory standards.

Responsible for managing operations and engagements within the Market Access team, ensuring strategic initiatives are executed effectively while analyzing business performance and collaborating with stakeholders.

The Regional Account Executive will drive territory growth through business development, build relationships with healthcare providers, and execute sales strategies for genetic testing services.

This role supports the Medical Science Liaison team by managing clinician inquiries, onboarding new clinicians, and organizing MSL communications, enhancing overall engagement and operational efficiency.

The role supports the Medical Science Liaison team by handling clinician communications, onboarding, and educational needs, improving workflow and engagement efficiency.

The Executive Director, Investor Relations leads the investor relations strategy, engaging with investors, managing communications, and advising leadership to enhance company value during clinical and commercial transitions.

Lead strategic new business for a SaaS data and analytics platform in the life sciences market, focusing on high-value partnerships with pharma and biotech companies, while shaping the market approach and influencing internal strategies.

The Regulatory Start-Up Associate is responsible for submissions to ethical and regulatory bodies during clinical trial start-up phases, ensuring compliance with regulations and guidelines. They coordinate with stakeholders to manage timelines and maintain trial data accuracy.

The Marketing Manager will lead provider education and lifecycle marketing, manage email campaigns, produce content, and build relationships to enhance partner engagement and retention.

The Senior Mobile App UI/UX Designer will create intuitive designs for mobile apps, collaborate with teams, improve user experiences, and maintain design systems.