Search the 11 jobs at Eikon Therapeutics

The Warehouse Associate 2 will support biotech operations by handling and moving materials and supplies efficiently. Responsibilities include receiving and verifying materials, operating forklifts, managing inventory, preparing shipments, maintaining records, and ensuring safety compliance within the warehouse environment.

The Associate Director, Drug Product will oversee the development and manufacturing processes of drug products, ensuring compliance with regulatory standards, managing cross-functional teams, and driving project advancements through early clinical to commercial stages. Responsibilities include formulation development, regulatory submissions, and mentoring junior staff.

As a Senior Software Engineer, you will collaborate with scientists to develop algorithms and software solutions for extracting and quantifying biological data from innovative imaging hardware. You will manage multiple projects, ensuring alignment with company goals and industry best practices.

As Associate Director, Bio-Markers, you will lead the discovery and utilization of biomarkers through collaboration with interdisciplinary teams, overseeing the identification, validation, and interpretation of biomarkers, and contributing to novel diagnostic and therapeutic approaches.

As a Senior Medical Writer, you will lead the authoring and editing of medical and regulatory writing deliverables that support clinical projects. Responsibilities include preparing regulatory documents, managing the document lifecycle, and collaborating with cross-functional teams to ensure adherence to guidelines and quality standards.

Collaborate with scientists and engineers to develop software solutions for biophysical problems and proprietary imaging-based datasets in a biopharmaceutical company focused on drug discovery.

The Facilities Coordinator will assist the facilities team by managing phone calls, greeting guests, ordering office supplies, and performing administrative tasks. Responsibilities also include monitoring security systems, managing badges, and handling work order tickets with the aim of ensuring a well-functioning work environment.

As Associate Director of Toxicology, you will lead non-clinical safety assessments to support clinical testing, design GLP compliant studies, analyze data, communicate results, and author regulatory documents. Strong collaboration and communication skills are vital for cross-functional team integration and regulatory interactions.

The Senior Counsel at Eikon Therapeutics will oversee the contracts function, provide legal guidance in areas such as privacy, employment, corporate governance, and healthcare compliance, and collaborate with various departments to support the organization's legal needs. This role requires a strong contract law background and the ability to manage a contracts team while advising on strategic transactions.

The Associate Director will manage the negotiation of complex agreements for global clinical trials, focusing on Clinical Trial Agreements. They will oversee third-party contract negotiations, ensure compliance, track contract performance, and collaborate with various teams on contracting and procedural improvements.

The Senior Research Associate 2 will execute experiments to support target discovery and validation for Parkinson's Disease. Key responsibilities include performing biochemical and cell-based assays, troubleshooting experiments, maintaining organized records, and ensuring adherence to safety and regulatory protocols.