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.

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.

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

The Director will lead site engagement and monitoring for clinical trials, ensuring high quality data delivery and effective collaboration with teams.

The Senior Medical Writer will lead the development of clinical and regulatory documents, ensuring accuracy and compliance while collaborating with cross-functional teams to manage project timelines and improve writing processes.

The Associate Director, Study Start-Up leads feasibility activities for clinical trials and ensures efficient study start-up, collaborating across teams and optimizing processes.

Lead the computer system validation and quality assurance efforts in biotech, ensuring compliance with regulatory standards, and managing the QA team.