Coordinate and manage CMC functional timelines across process development, manufacturing, QC/QA, and assay development. Support meeting facilitation, follow-up on actions, escalate risks, prepare internal reports and materials, and assist translational teams to progress toward GMP manufacturing and clinic.
Adverum Biotechnologies, Inc. is a mission-driven clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocular diseases with the aspiration of developing functional cures to restore vision and prevent blindness. Leveraging the research capabilities of its proprietary intravitreal (IVT) platform, Adverum is developing durable, single-administration therapies designed to be delivered in physicians’ offices to eliminate the need for frequent ocular injections to treat these diseases. By overcoming the challenges associated with current treatment paradigms for these debilitating ocular diseases, Adverum aspires to transform the standard of care, preserve vision, and create a profound societal impact around the globe.
Note to Recruiters and Agencies
All recruiter and agency inquiries must go through Adverum’s internal Talent Acquisition team. Unsolicited resumes sent to Adverum will be considered Adverum's property. Adverum’s Talent Acquisition team must expressly engage agencies for any requisition. Direct contact with hiring managers by agencies will not be tolerated and may affect your ability to work with Adverum in the future.
What you'll do:
- Manage functional CMC timelines (e.g. Process Development, External Manufacturing, Quality Control, Quality Assurance, Assay Development), coordinating with functional leads on key tasks to ensure on-track delivery
- Support CMC Lead and functional leads in agenda coordination for team and cross-functional meetings; attend meetings, generating clear minutes with actions and decisions well-documented
- Follow up on action items to ensure progress
- Disseminates and facilitates information flow/exchange among CMC Functions
- Work with team members to escalate constraints, risks, and conflicts via appropriate internal channels
- Provide support for internal reporting, generating materials (e.g. slides, gantt charts, excel sheets) to facilitate discussion and leadership presentations
- Support Research and Non-clinical teams on timelines, ensuring translational work can progress towards GMP Manufacturing and the clinic
About you:
- 1-2 years of project management experience of Technical Project Management in the Pharma CMC space
- Proficient with Microsoft Office, Microsoft Project
- Experience with Timeline Management and Meeting Facilitation
- Experience working with vendors/clients
- Laboratory experience/exposure
- Ability to travel for work-related projects
At Adverum, Inclusion and Diversity are at our core. We believe in the power of being your authentic self. We strive to create the space that allows for everyone in our Adverum Community to not only feel safe but also encouraged to speak, learn from each other, grow in their professions, and be the very best versions of themselves no matter what their age, ethnic background, gender, origin, religion or sexual orientation.
Top Skills
Excel
Gantt Charts
MS Office
Microsoft Project
PowerPoint
Adverum Biotechnologies Redwood, California, USA Office
100 Cardinal Way, Redwood, CA, United States, 94063
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