Manager / Senior Manager, Clinical Project Management
Artiva Biotherapeutics · San Diego, CA · 1 mo ago
On-siteInformation Technology$130k–$180k/yrFull-time
Duties/Responsibilities
- Timeline Tracking and Integration
- Responsible for creating, maintaining and communicating cross-functional development project management plans at the task, study and molecule levels
- Responsible for producing cross functional Project Management tools/visuals/GANTS as required in support of the development team in industry standard software packages
- Communicating changes, impacts and potential mitigations across the development team and working to align the cross functional team on best path forward
- Support to the finance organization regarding timeline models, changes, and Financial Planning and Analysis integration
- Communication across internal teams and external stakeholders
Risk & Issue Management
- Identify, assess, and track cross-functional risks and dependencies across the development team space
- Communicate to higher organizational structures status, timeline changes and impacts to cross functional deliverables to support mitigation planning
- Develop and maintain the cross-functional risk register for the development team
- Ensure timely tracking and modeling of the impact of critical risks impacting program timelines, quality, or strategic milestones
- Support leadership governance activities through preparation of timeline models and scenarios in support of risk assessments.
Data Tracking & Reporting
- Develop and maintain dashboards to support development team in data tracking and communication to Senior Management
- Prepare clear, concise program updates for cross-functional teams and leadership
- Ensure consistent reporting across ongoing clinical studies
Governance & Communication
- Support cross-functional governance meetings, including agenda setting, materials preparation, decision tracking, and follow-up actions
- Drive accountability across teams for agreed-upon deliverables