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5 дней назад

Associate Director, Program Management Leader (Clinical Research)

96 000 - 165 025
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
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 Research): Translating compound development strategies into integrated development plans and leading cross-functional program management teams with an accent on pharmaceutical development, clinical research operations, budgeting, and risk management. Focus on navigating complex drug development programs, securing resources, managing execution across Phase I–IV studies, and building high-performing global teams.

Location: Hybrid role in Beerse, Antwerp, Belgium; up to 20% domestic and international travel required.

Base pay: €96,000–€165,025 annually, plus an annual bonus and location-dependent benefits.

Company

Johnson & Johnson Innovative Medicine develops medicines and healthcare solutions across the spectrum from research to patient care.

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 functional areas.
  • Define and monitor program scope, timelines, budgets, resources, risks, and mitigation strategies.
  • Guide cross-functional teams through the pharmaceutical and clinical development process and governance reviews.
  • Maintain risk-management registers, manage changes, and drive issue resolution.
  • Build a trusted, high-performing team environment with clear accountabilities, decision rights, and communication pathways.

Requirements

  • Bachelor’s degree required, preferably in life sciences; an advanced degree is preferred.
  • 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, and clinical trial execution.
  • Strong communication, presentation, interpersonal, leadership, analytical, decision-making, and financial management skills.
  • Ability to lead without authority in multifunctional and global matrix environments.

Nice to have

  • Project Management certification such as PMP or CPM.
  • Experience across Phase I–IV studies.
  • Oncology therapeutic-area experience.
  • Mentoring and coaching experience.
  • Experience in early therapeutic area leadership, disease or pathway area strategy, or licensing and acquisitions program management.

Culture & Benefits

  • Inclusive work environment focused on individual contribution, diversity, and dignity.
  • Vacation days, parental leave of at least 12 weeks, bereavement leave, caregiver leave, and volunteer leave.
  • Well-being reimbursement and financial, physical, and mental health programs.
  • Service anniversary and recognition awards.
  • Eligibility for insurance plans and an annual performance-based bonus, subject to local terms.

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