Eikon Therapeutics Jobs

Own global investigator site budget strategy, development, benchmarking, and negotiation, including CTA execution and FMV documentation for oncology studies. Coordinate with internal teams and vendors, manage start-up performance and risks, and improve processes to accelerate site activation while ensuring compliance. Requires at least 10 years of experience with a bachelor’s degree or 8 years with a postgraduate degree, plus extensive clinical operations, study start-up, or investigator site budget experience. Candidates should have expertise in protocol-based procedure-level budgeting, FMV principles, clinical trial start-up, project management, and Veeva Vault Clinical; oncology experience and relevant certifications are preferred.