Top Remote Pharmaceutical Jobs in Chicago, IL

Design and implement ETL/ELT data pipelines, optimize performance, ensure data quality, and collaborate with data teams to create solutions for analytics.

Support complex technical issue resolution for customers, liaise between product owners and development teams, and improve commercial technologies.

The Director of Data Engineering will lead the engineering team in building a scalable data platform, ensuring data quality and compliance, while collaborating with various stakeholders to enhance analytics capabilities.

Lead secure design and architecture initiatives for product security, ensuring compliance with security policies and collaboration with teams across the product lifecycle.

The Business Development Manager will manage customer outreach, explore business opportunities, negotiate contracts, and support marketing efforts in the biotech field.

The Associate Director will develop and implement strategic plans, oversee operations, improve processes, manage budgets, and collaborate across functions in Global Medical Affairs.

The Clinical Research Associate will monitor clinical trial sites, ensure compliance with protocols and regulations, and support site staff while managing multiple projects.

As a Clinical Research Associate at ICON, you will design and analyze clinical trials, ensure protocol compliance, and collaborate with site staff for effective study conduct.

The Clinical Research Associate will manage clinical trial activities, ensuring adherence to protocols and standards, and conducting site visits while overseeing data integrity and participant safety.

The Sr. Clinical Research Associate manages sites for clinical trials, ensuring compliance with protocols and regulations, conducting monitoring visits, and collaborating with study teams.

The Senior Clinical Research Associate manages study sites, ensuring compliance with regulations and high performance. Responsibilities include site selection, monitoring, training site staff, and data management.

Manage end-to-end labeling operations across global markets, ensure compliance with regulatory requirements, coordinate teams, and oversee drug safety activities.

The role involves leading a team in design and human factors engineering for delivery devices, ensuring compliance with regulations and enhancing product innovation.

The Associate Director of Product Management at Lilly.com leads cross-functional teams to define and execute the product strategy, ensuring customer-centric digital solutions while driving engagement and compliance in the life sciences sector.

The Design Lead will guide the creation of innovative digital experiences, contributing to strategic design projects while collaborating across teams to deliver compelling visual solutions.

The Director of Key Account Management drives strategic growth and partnerships within the Cell & Gene Therapy segment, influencing executive relationships and ensuring client alignment on business strategies.

The Director is responsible for optimizing market access strategy for product launches by collaborating across various teams to ensure effective execution and delivery of strategies for payer coverage and affordability.

Manage TMF documentation transitions within Novartis for M&A and licensing projects, ensuring compliance and process improvement in clinical document management.