Clinical Trial Manager

Role: Clinical Trial Manager supporting one or more clinical studies within a biopharma environment, primarily overseeing operational aspects to ensure compliant and timely trial execution. Responsibilities: manage vendor and site activities, oversee site initiation, patient enrollment, and data accuracy; monitor site performance and compliance with GCP and regulations; support study documentation, vendor management, and internal/external reporting; and contribute to process improvements. Qualifications: Bachelor’s degree in a scientific field; 5+ years of industry experience with at least 2 years in trial management, preferably in oncology; thorough understanding of clinical trial processes, ICH GCP guidelines, and relevant regulations. Core skills include strong organizational, communication, and negotiating abilities, proficiency with clinical trial management systems (e.g., EDC, CTMS, eTMF), and ability to work independently. HighValue: experience managing oncology trials, familiarity with trial start-up through closure, and vendor oversight. Work setup is flexible, with options for remote or hybrid based in Hayward or Brisbane, CA; travel is expected at 10-20% domestically and internationally.