7 часов назад
Senior Program Management Director (Biotechnology)
204 500 - 290 500$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Program Management Director (Biotechnology) (Drug Development): Managing complex biotechnology development programs from discovery and translational research through clinical phases, CMC, and NDA/BLA filings with an accent on cross-functional strategy, integrated planning, and governance. Focus on overseeing portfolios, identifying risks and dependencies, managing resources and budgets, and driving alignment across scientific, regulatory, and commercial stakeholders.
Location: Alameda, California, United States; onsite office-based role
Salary: $204,500–$290,500 annually, with eligibility for a discretionary annual bonus.
Company
is a biotechnology company developing medicines across discovery, clinical development, CMC, regulatory filings, and post-approval programs.
What you will do
- Oversee complex discovery, translational research, CMC, clinical development, filing, approval, and post-approval programs.
- Develop integrated cross-functional project plans, Gantt charts, timelines, status reports, and strategic development and filing plans.
- Manage dependencies, critical paths, resources, budgets, governance approvals, risks, and contingency plans.
- Partner with project leaders, team leaders, finance, and cross-functional teams to define and execute product development strategies.
- Communicate recommendations and program status to executive leadership and governance bodies.
- Lead department-level and cross-functional initiatives to improve processes and establish best practices.
Requirements
- BS/BA in STEM with at least 15 years of relevant experience, MS/MA with at least 13 years, or PhD with at least 12 years.
- 12–15 years of experience managing cross-functional teams in the biotech or pharmaceutical industry, including CMC, discovery, or development.
- Extensive understanding of the full drug development process, including discovery, CMC, development, and regulatory filing.
- Strong analytical, communication, presentation, collaboration, negotiation, leadership, influencing, and organizational skills.
- Ability to manage multiple complex projects and process significant amounts of information while maintaining attention to detail.
- High proficiency with MS Office Suite, Planisware, MS Project, or equivalent project management software.
Nice to have
- Experience managing small molecules or biologics in cancer immunology or oncology.
- Experience with corporate partnerships, alliance management, or business development deals.
- Experience across at least two different drug development functions or phases.
Culture & Benefits
- Collaborative office environment designed to support close team interaction and idea sharing.
- Equipment includes dual monitors and ergonomic chairs.
- Employee benefits include 401(k) contributions, medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
- Benefits include stock purchase opportunities, long-term incentives, 15 accrued vacation days in the first year, 17 paid holidays, a company-wide winter shutdown, and up to 10 sick days.
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