Clinical Trials Manager I

Role: Clinical Trials Manager I supporting Cytokinetics' cardiovascular biopharma pipeline, primarily focused on clinical operations for Phase II or III studies. Responsibilities: coordinate all study activities, ensure compliance with FDA and ICH-GCP guidelines, manage CROs and vendors, oversee study start-up, conduct, and close-out processes, and maintain documentation quality. Collaborate with cross-functional teams including finance and vendors, and participate in study meetings. Qualifications: BA/BS in a science-related field; 1-3 years of clinical research experience, preferably sponsor-side; strong communication, problem-solving, and organizational skills; basic knowledge of regulatory guidelines; proficiency in MS Office; willingness to travel (~20%). HighValue: supports cardiovascular drug development, Phase II/III, clinical operations, vendor management, regulatory compliance, documentation, sponsor experience preferred, on-site in South San Francisco with travel. WorkSetup: onsite, approximately 20% travel.