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9 дней назад

Clinical Program Manager (Biotech)

182 070 - 235 620$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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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