9 дней назад
Clinical Program Manager (Biotech)
182 070 - 235 620$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Clinical Program Manager (Biotech): Leading the execution of Phase I–IV clinical trials and clinical operations programs with an accent on study budgets, timelines, resource management, CRO oversight, and regulatory compliance. Focus on leading cross-functional study teams, managing risks and vendors, developing clinical documentation and SOPs, and coaching direct reports.
Location: United States, California, Foster City
Salary: $182,070–$235,620 per year for the Bay Area; $165,495–$214,170 per year in other US locations. Additional eligibility may include an annual bonus, long-term stock incentives, paid time off, and benefits.
Company
Develops cancer immunotherapies, including CAR T-cell and T-cell receptor engineered cell therapies, to provide durable responses and reduce the burden of chronic care.
What you will do
- Lead the successful execution of one or more Phase I–IV clinical studies and programs within defined budgets and timelines.
- Manage direct and potentially indirect reports, including hiring, coaching, development, performance management, and retention.
- Lead cross-functional Study Management Teams and influence stakeholders across Clinical Operations and related functions.
- Manage study resources, project timelines, budgets, risks, issues, and mitigation plans.
- Oversee CRO and vendor selection and management, including requests for proposals.
- Develop and maintain study protocols, regulatory documentation, SOPs, training, and process improvements in line with applicable regulations.
Requirements
- Bachelor’s degree with eight years of experience, master’s degree with six years of experience, or PhD/PharmD.
- Cross-functional study management or related leadership experience in life sciences, including experience managing study or project teams.
- Experience starting, managing, and closing clinical studies and authoring clinical study, regulatory, and SOP documentation.
- Knowledge of FDA, EMA, ICH, GCP, and other applicable national regulations.
- Ability to lead and influence programs, manage change, coach others, and work effectively in a highly matrixed environment.
- Ability to travel when needed.
Culture & Benefits
- People leadership focused on inclusion, talent development, team empowerment, and career growth.
- Medical, dental, vision, and life insurance plans for eligible employees.
- Paid time off and potential discretionary annual bonus and stock-based long-term incentives.
- Work supporting innovative cancer therapies and global clinical development programs.
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