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обновлено 2 дня назад

Senior Legal Counsel, R&D Legal EMEA (MedTech)

96 000 - 165 025€
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
c1
Страна
Belgium

Описание вакансии

Текст:
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TL;DR
Senior Legal Counsel, R&D Legal EMEA (MedTech): Providing strategic legal guidance for clinical development, research collaborations, and related agreements across EMEA with an accent on risk assessment, regulatory compliance, and practical business counseling. Focus on interpreting clinical research regulations, negotiating complex cross-border agreements, and guiding R&D stakeholders through evolving legal and compliance issues.

Location: Hybrid role based in Diegem or Beerse, Belgium

Base pay: €96,000–€165,025 annually

Company

Johnson & Johnson MedTech develops healthcare and medical technology solutions as part of Johnson & Johnson’s global healthcare business.

What you will do

  • Provide strategic legal guidance for early- and late-stage clinical trials, investigator-initiated studies, collaborative research, and other R&D initiatives across EMEA.
  • Support program, portfolio, and study-level reviews by identifying legal and compliance risks and advising on mitigation strategies.
  • Interpret applicable laws, regulations, industry codes, GCP requirements, ICH Guidelines, GXPs, and company policies.
  • Draft, review, and provide legal oversight for clinical research agreements and related documentation.
  • Support contract negotiations, issue resolution, escalation pathways, governance forums, and legal training materials.
  • Collaborate with R&D, clinical operations, regulatory, compliance, privacy, tax, medical affairs, and other functions.

Requirements

  • Master of Laws degree with excellent academic results.
  • At least 7 years of legal experience, including at least 5 years supporting R&D, clinical development, life sciences, healthcare, or another highly regulated industry.
  • Practical experience advising on clinical research, clinical development, external research collaborations, or related R&D activities.
  • Experience conducting legal risk assessments and advising on program, portfolio, or study-level matters in a regulated environment.
  • Strong knowledge of national and European R&D and clinical research laws, regulations, industry standards, ICH Guidelines, and GXPs.
  • Fluent written and spoken English required. Experience in multinational corporations and healthcare is preferred.

Culture & Benefits

  • Inclusive, diverse, and multidisciplinary working environment.
  • Hybrid work arrangement with collaboration across regional and global teams.
  • Annual bonus based on pay grade, location, and company and employee performance.
  • Vacation, parental, bereavement, caregiver, and volunteer leave.
  • Well-being reimbursement and financial, physical, and mental health programs.
  • Insurance plans, service anniversary awards, and recognition programs subject to applicable plan terms.