Top Tech Jobs & Startup Jobs in Austin, TX

The Clinical Supply Support Specialist manages supply monitoring, procurement of comparator drugs, shipment coordination, documentation updates, and IRT management activities to support clinical trials.

The Regulatory Affairs Consultant guides clinical studies through regulatory requirements, advising teams on compliance and strategies for efficient trial execution. They engage with health authorities, manage communication, and ensure quality documentation.

The Senior Clinical Research Associate manages clinical trial sites, ensures adherence to regulations, oversees study conduct, and resolves issues while safeguarding patient safety.

The Executive Director, HEOR Modeling leads HEOR consulting projects, manages staff, ensures client satisfaction, and drives AI integration in HEOR while overseeing business development and strategic planning.

Lead lab operations by enhancing efficiency, managing projects, ensuring data integrity, and supporting clinical trials through effective programming and analysis.

The Senior Regulatory Consultant will oversee regulatory strategies, manage complex timelines, enhance team performance, and guide regulatory projects to support the development of transformative therapies.

As a Senior/Principal Regulatory Compliance Consultant, you will lead client engagements in QC Microbiology and sterile drug manufacturing, ensuring compliance and quality improvements while traveling extensively to support clients.

The Senior Clinical Research Associate is responsible for site management, monitoring clinical trials for compliance with regulations, ensuring patient safety, and resolving issues at investigator sites.

The Senior Clinical Research Associate oversees site management and monitoring for clinical trials, ensuring compliance with GCP, patient safety, and quality execution of studies. Responsibilities include managing operational aspects, training site personnel, addressing protocol issues, and conducting monitoring activities.

The Senior Clinical Research Associate manages site monitoring and relationships for clinical trials, ensuring compliance and patient safety according to GCP and regulations.