Clinical Trial Manager

Role: Clinical Trial Manager overseeing Phase I-III oncology trials in a late-stage biopharma focused on RAS-targeted therapies for RAS-mutant cancers. Responsibilities: manage CROs, ensure trial execution aligns with GCP, FDA regulations, and SOPs; develop study documentation; monitor study progress, site activities, and investigator relationships; oversee trial documentation and budgets; collaborate across departments including Regulatory, Clinical Development, QA, and vendors; support safety reporting and data integrity; mentor CRAs; and serve as primary contact for study teams. Requirements: BS/MS with 5+ years in clinical operations, preferably within oncology drug development; strong knowledge of FDA, ICH, GCP; experience managing CROs and vendor relationships; excellent communication skills; ability to travel (~25%). Preferred: experience with global studies, cooperative group trials, investigator-sponsored trials, and familiarity with Asia-Pacific regions. High-value biopharma specifics include early to late-phase clinical trial management, biologics targeting RAS mutations, and a focus on precision oncology therapeutics. Work setup: onsite at Redwood City, CA, with a competitive salary range of $120,000–$150,000, including benefits and equity.