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The Senior Director of Drug Safety and Toxicology will lead safety assessments, manage toxicology studies, and author regulatory documents while ensuring compliance with guidelines during project phases.

The Senior Research Associate II will conduct cell culture experiments, support target validation for Parkinson's disease, and maintain detailed records.

Lead procurement and supply chain functions to develop and execute strategies for sourcing, supplier management, and logistics within Eikon Therapeutics.

The EHS Specialist 2 will plan, implement, and enforce EHS policies, manage training, handle hazardous materials, and ensure compliance with regulations.

The Principal Engineer will design and support computational pipelines for analyzing microscopy data while leading a multidisciplinary team and maintaining architectural vision.

The Service Technician will respond to service requests, maintain lab equipment, document work, and ensure safety compliance.

Manage regulatory affairs, ensuring compliance with FDA and international standards, oversee submissions, and collaborate with cross-functional teams on product development.

The Manager, TMF Operations oversees the Trial Master File ensuring accuracy and compliance, working with clinical teams, and managing TMF documentation for regulatory readiness.

Manage regulatory clinical trial applications and compliance efforts, ensuring biotechnological innovations adhere to regulations while collaborating with cross-functional teams for submissions and strategic planning.

The Senior Manager, Statistical Programming will oversee statistical programming deliverables in clinical studies, ensuring quality and compliance while leading teamwork and operational excellence.