Associate Clinical Trial Manager

Job Summary

Supporting the implementation and conduct of clinical research projects, the full-time Associate Clinical Trial Manager will manage large global oncology clinical trials, assist with clinical vendors, and oversee Trial Master File activities, working either onsite in San Diego or remotely.

Key responsibilities

• Manage or assist in the management of large global oncology clinical trials (Phase 1-3) ensuring compliance with protocols and regulations
• Track study progress, maintain status updates, and provide progress reports to project teams
• Maintain and support the eTMF for clinical studies, ensuring proper documentation and compliance

Required qualifications

• Undergraduate degree in Biological Sciences or related fields with 1-2 years of relevant experience
• 1-2 years of experience in clinical operations within a pharmaceutical company or CRO
• Experience in TMF/document management or clinical trial support
• Familiarity with eTMF systems such as Trial Interactive eTMF or Veeva Vault
• Knowledge of ICH-GCP guidelines and regulatory requirements