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5 дней назад

Associate Director, Program Management Leader (Clinical Trials)

137 000 - 235 750$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US/Belgium
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Associate Director, Program Management Leader (Clinical Trials): Translating compound development strategy into development plans and leading cross-functional program execution with an accent on clinical research operations, budget management, and risk mitigation. Focus on coordinating project managers, navigating pharmaceutical development decisions, and maintaining program delivery across complex global teams.

Location: Hybrid role based in Raritan, New Jersey; Spring House, Pennsylvania; or Beerse, Belgium. Up to 20% domestic and international travel required.

Salary: $137,000–$235,750 base pay annually.

Company

Johnson & Johnson develops innovative medicines and MedTech solutions across the healthcare spectrum.

What you will do

  • Translate Compound Development Team strategy into Compound Development Plans and operational execution plans.
  • Lead the Program Management Team and coordinate project managers across cross-functional disciplines.
  • Establish and monitor program scope, timelines, budgets, resources, assumptions, and cost estimates.
  • Identify operational risks, maintain risk-management registers, and drive issue mitigation and change management.
  • Guide teams through pharmaceutical and clinical development processes, governance reviews, strategy approval, and resource allocation.
  • Build a high-performing, collaborative team environment with clear accountabilities, decision rights, communication, and escalation pathways.

Requirements

  • Bachelor’s degree required; a Life Science degree is preferred, and an advanced degree is advantageous.
  • At least 8 years of experience in the pharmaceutical, CRO, or related healthcare industry.
  • Experience with pharmaceutical development, clinical research operations, and R&D project management.
  • Knowledge of project management systems, methodologies, tools, financial management, and clinical trial execution.
  • Strong communication, presentation, interpersonal, leadership, analytical, negotiation, and decision-making skills.
  • Ability to lead without authority in multifunctional, matrixed, and global environments.

Nice to have

  • Project Management certification such as PMP or CPM.
  • Experience across Phase I–IV studies and in the oncology therapeutic area.
  • Experience mentoring or coaching others.
  • Experience with early therapeutic area leadership, disease or pathway area strategy, or licensing and acquisition programs.

Culture & Benefits

  • Hybrid work environment with domestic and international collaboration.
  • Participation in pension, 401(k), and long-term incentive programs.
  • Vacation, sick time, holidays, personal and family time, parental leave, caregiver leave, bereavement leave, volunteer leave, and military spouse time off.
  • Inclusive workplace and interview process with accommodation support for applicants with disabilities.

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