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.
Eikon Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
