Search the 7 jobs at Eikon Therapeutics

The Senior Counsel at Eikon Therapeutics will manage the legal department's contracts function and provide counsel on various legal matters including privacy regulations, employment law, corporate governance, and healthcare compliance. The role involves collaborating with leadership and legal teams to support the company's strategic initiatives while overseeing a contracts team and managing outside counsel.

As a Senior Medical Writer at Eikon Therapeutics, you will author and edit regulatory documents related to clinical studies, collaborate with various teams for high-quality documentation, manage document lifecycles, and ensure compliance with regulatory standards, while continuously improving writing processes.

As a Senior Software Engineer, you will develop algorithms and computational solutions to analyze high-content biological datasets. Responsibilities include collaborating with scientists, implementing software solutions, and managing multiple projects aligned with company goals.

The Associate Director, Drug Product oversees drug product development and manufacturing, ensuring compliance with regulatory standards, while leading cross-functional teams to enhance the company's product pipeline from early clinical stages to commercial production.

As a Software Engineer 2, you will collaborate with interdisciplinary teams to develop computational solutions for analyzing and quantifying scientific datasets. You'll contribute to novel algorithms for biophysical problems, guide software through its lifecycle, and manage multiple projects to meet company objectives.

The Associate Director, Contracts Professional will manage the negotiation of complex clinical trial agreements and oversee third-party contract negotiation resources. This role includes ensuring compliance with regulations, maintaining vendor relationships, tracking performance metrics, and improving contracting processes.

The Senior Research Associate 2 will execute experiments supporting target discovery and validation for Parkinson’s Disease. Responsibilities include conducting biochemical and cell-based assays, troubleshooting experiments, and maintaining laboratory records and equipment. A strong emphasis on safety and regulatory compliance is required.