Top Tech Jobs & Startup Jobs in Seattle, WA

The Clinical Monitoring Manager oversees in-house CRAs and CROs for clinical trials, ensuring compliance and quality. They manage and support clinical study activities, liaise with stakeholders, and ensure trial readiness.

The Associate Director will lead late-stage development and commercialization of monoclonal antibodies, focusing on process delivery and oversight with CDMO partners.

The Senior Manager will manage operational and planning aspects of medical congress and publication activities, ensuring compliant delivery of scientific communication materials and cross-functional collaboration.

Manage the end-to-end clinical supply chain for multiple clinical programs, ensuring timely delivery of products while collaborating with various cross-functional teams and maintaining regulatory compliance.

Lead statistical programming for clinical trials, managing programmers and CROs. Oversee programming activities, ensuring timely support for clinical projects and developing programming processes.

The Director of GMP Quality Assurance will ensure quality compliance in biologics manufacturing, oversee audits, manage batch releases, and drive continuous improvement in quality systems.

The Associate Director leads QC analytical testing, ensuring compliance with regulations, managing method validations, and collaborating on regulatory submissions.

The Senior Manager, Regulatory Affairs will oversee regulatory strategies, manage submissions to the FDA and international agencies, and coordinate with cross-functional teams to ensure compliance and timely submissions.

Manage logistics of biomarker sample collection, ensure adherence to clinical protocols, oversee data transfer, vendor management, and budget tracking for clinical trials.

The Senior Manager of Clinical Systems oversees clinical technology initiatives, manages clinical systems projects, ensures compliance, and promotes process adoption across multiple functions while collaborating with various stakeholders.