Clinical Trial Manager

Role: Clinical Trial Manager supporting clinical study operations in a pharmaceutical setting, primarily focused on clinical trial delivery, vendor oversight, and compliance. Responsibilities include managing day-to-day trial activities, overseeing site and vendor performance, ensuring regulatory adherence (ICH GCP, FDA regulations), and supporting study documentation, data integrity, and site initiation procedures. The role involves collaboration with CROs, internal teams, and external vendors, along with monitoring trial progress and quality. Qualifications: Bachelor’s degree in a scientific field; 5+ years in the pharmaceutical industry with at least 2 years in trial management, preferably in oncology; strong understanding of clinical trial processes, GCP, and regulatory standards. Skills include excellent organization, communication, and negotiation abilities; proficiency in clinical trial management systems (EDC, CTMS, eTMF); and ability to travel 10-20%. High-value specifics: trial management in oncology, phase 1-3 or late-stage studies, vendor and site oversight, remote or hybrid work based in California, with a salary range of $120,000–$135,000.