Jobs at Eikon Therapeutics

Leads global investigator site budget development and clinical trial agreement negotiations across oncology studies. Builds procedure-level budgets, applies fair market value principles, manages country-specific templates, and oversees CTA execution. Partners with Clinical Operations, Legal, Finance, Regulatory, vendors, CROs, and investigative sites to accelerate activation timelines. Owns contracting metrics, forecasting, escalation processes, compliance, and process improvements, while potentially coaching study start-up and contracting teams.

Manages day-to-day laboratory operations supporting scientific and engineering teams. Responsibilities include inventory and vendor management, equipment installation and maintenance, calibration, asset documentation, lab support activities, cell culture environment upkeep, laboratory gases, cold storage, waste disposal, safety compliance, SOP maintenance, space planning, and operational troubleshooting. The role also coordinates with Facilities, EH&S, IT, Procurement, vendors, and research teams to improve efficiency, reliability, and cost control.

Design, implement, and maintain informatics systems (LIMS/ELN, inventory, data lake) and AI/ML-enabled workflows to support R&D. Build ETL pipelines, integrate systems, gather requirements from scientists, document architectures, train users, and contribute to enterprise data platform and automation to accelerate research decision-making.

Perform high-throughput and supercritical fluid chromatography (SFC) purification of small molecules, run mass-directed purification on Waters and Agilent systems, maintain and troubleshoot preparative/analytical instruments, manage large sample sets and data, compile and present results, and collaborate with medicinal chemistry to optimize purification workflows and inventory management.

Lead design, deployment, and maintenance of enterprise IT systems and data center operations. Provide expert technical support, security incident response, patching, backup/recovery, inventory and access management, and documentation. Collaborate cross-functionally, mentor junior staff, and improve onboarding/offboarding and operational processes to ensure infrastructure reliability and security.

Lead regulatory strategy and compliance for biopharmaceutical product development. Oversee preparation and submission of INDs/NDAs/MAAs, ensure GCP/GLP compliance, assess regulatory risk, liaise with agencies, and collaborate with R&D, QA, and clinical teams to support approvals and commercialization.

Lead strategy, design, governance, and execution of Total Rewards programs (compensation, equity, benefits, recognition). Partner with Executive Leadership, Board Compensation Committee, Finance, Legal, and HR to ensure compliance, compensation governance, and competitive programs. Build and develop a Total Rewards team, manage benefits vendors, own equity strategy and SEC-related disclosures, and drive HRIS/compensation planning tools and analytics to support workforce planning and communications.

The Director, Regulatory Affairs will lead regulatory strategy and execution for clinical development programs, ensuring compliance with FDA and international regulations, and collaborating with cross-functional teams.

Lead statistical design, analysis, and reporting for clinical trials and experimental studies. Develop statistical analysis plans, perform advanced analyses (including Bayesian and adaptive designs), mentor biostatisticians, contribute to regulatory submissions and publications, and drive adoption of statistical tools within cross-functional teams.