Clinical Trials Manager I
Cytokinetics · South San Francisco, CA
Clinical OperationsFull-time$124k–$145kCompany career page
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Role summary
Cytokinetics seeks a Clinical Trials Manager I to support operational coordination and oversight of clinical trials for cardiovascular programs. Working under senior guidance, the role ensures regulatory compliance, manages study logistics, and coordinates with cross-functional teams and vendors throughout trial execution.
What they're looking for
- Bachelor's degree in science-related field
- 1-3 years clinical research experience (CRA, Clinical Trial Associate, or equivalent)
- Strong written and verbal communication skills
- Basic understanding of ICH-GCP and FDA regulatory requirements
- Proficiency with Microsoft Office applications
- Ability to travel approximately 20% of the time
- Problem-solving skills and ability to work under pressure
What you'll be doing
- Manage multiple clinical studies in accordance with regulatory guidelines and internal SOPs
- Participate in design of study documents including protocols, case report forms, and informed consent forms
- Coordinate CRO and vendor activities including material shipment and site regulatory package preparation
- Support study management meetings and cross-functional team collaboration across phases
- Oversee study operations from start-up through close-out to ensure timely and budget-compliant execution
Privacy & handoff
This role links to Cytokinetics's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.