Назад
Company hidden
6 дней назад

Associate Director, Central Monitor

141 500 - 268 500$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
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
Associate Director, Central Monitor (Clinical Research/RBQM): Leading Central Monitoring Managers and staffing strategies for clinical research programs with an accent on risk-based quality management, study de-risking, and delivery excellence. Focus on building leadership pipelines, managing cross-functional teams, and making data-driven decisions across complex clinical studies.

Location: Hybrid; on-site Tuesday–Thursday. Candidates must be local to Lake County, Illinois; Irvine, California; or Florham Park, New Jersey.

Salary: $141,500–$268,500 per year, plus eligibility for short-term incentive programs.

Company

hirify.global develops medicines and solutions for serious health issues across immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Lead and supervise Central Monitoring Managers responsible for a portfolio of clinical studies.
  • Develop and execute central monitoring staffing strategies aligned with study priorities, timelines, quality, and efficiency.
  • Build the internal leadership talent pipeline through recruiting, coaching, mentoring, and training.
  • Manage performance cycles, including expectations, objectives, feedback, development, and performance issues.
  • Collaborate with Clinical Development Operations and cross-functional stakeholders to deliver high-quality outcomes.
  • Promote risk-based quality management and early detection of risks to de-risk clinical studies.

Requirements

  • Bachelor’s degree in life sciences, a related field, or a risk-based discipline.
  • At least 10 years of clinically related or data trend analysis experience, including 5 years of people management experience.
  • Required experience with an RBQM model or similar risk-based monitoring experience.
  • Experience with drug development, clinical operations, risk management, strategic execution, and decision-making.
  • Strong English skills in spoken, written, and conversational communication.
  • Strong analytical, critical thinking, planning, organizational, presentation, and stakeholder management skills; proficiency with data analytics, visualization tools, and Microsoft Office.

Culture & Benefits

  • Inclusive environment focused on collaboration, innovation, learning, and continuous improvement.
  • Benefits may include paid vacation, holidays, sick leave, medical, dental, and vision insurance.
  • Eligible employees may participate in a 401(k) plan and short-term incentive programs.
  • Leadership development is supported through coaching, mentoring, and continuous feedback.

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