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Associate Director / Director, Clinical Program Management
Company | Vividion Therapeutics, Inc. |
Address | San Diego, CA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Internet Publishing |
Expires | 2023-08-05 |
Posted at | 10 months ago |
Company Overview:
- Serve as primary PM for the Clinical Development team, including development and maintenance of strategic plans, timelines, and budgets.
- Support and collaborate with other cross-functional teams as needed.
- Develop and administer project status tools (e.g., dashboards, reports, templates, business processes) to assess project team performance.
- Lead project and program meetings, study meetings, and clinical team meetings: develop meeting agendas, prioritize topics, summarize decisions, and action items.
- Drive cross functional communication and decision making to ensure alignment with internal and external stakeholders.
- Work closely with Finance to generate budget forecasts in alignment with Clinical Development Plan.
- Support Compound Development Team Leader to provide PM end support, including to communicate key compound risks, and working with team to mitigate risk factors.
- Oversee external vendor activities including adherence to timelines, contracts, and budgets, along with invoicing process.
- Effective troubleshooting and problem-solving skills
- Expertise in a functional area directly contributing to successful mid to late-stage drug development
- Knowledge of the drug development process
- Experience with Project Management Software (SmartSheet, MS Project, ThinkCell, and OfficeTimeline)
- Familiarity with FDA and/or EMA Regulations, ICH Guidelines, and GCP governing clinical development activities.
- Excellent oral and written communication skills
- Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, SharePoint)
- Be an effective team player and strong individual contributor, flexible, and able to handle multiple tasks and deliver high-quality results under tight timelines
- BA/BS in a scientific field plus 8-10 years of pharmaceutical/clinical development experience, including a minimum of 5-6 years project/program management experience
- Phase 1/2 Clinical study experience highly preferred
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