8 часов назад
Director, Global R&D, Clin/Med and BD
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Director, Global R&D, Clin/Med and BD (Healthcare Compliance): Leading the global Health Care Compliance program across clinical research, medical affairs, R&D, and business development with an accent on risk-based compliance, strategic transactions, and regulated healthcare activities. Focus on advising senior leaders, conducting pre-acquisition compliance due diligence, and designing scalable compliance solutions across regions.
Location: Hybrid role based in Zug, Switzerland; travel up to 20–30%.
Company
Johnson & Johnson MedTech develops healthcare solutions and medical technologies focused on preventing, treating, and curing complex diseases.
What you will do
- Lead the global Health Care Compliance program for Clinical Research, Medical Affairs, R&D, and Business Development.
- Design and enhance risk-based compliance programs covering clinical trials, investigator and site interactions, research collaborations, scientific exchange, and strategic transactions.
- Advise senior R&D, Clinical, Medical Affairs, and Business Development leaders on compliant business models, collaborations, and growth initiatives.
- Lead compliance due diligence for acquisitions, investments, joint ventures, partnerships, licensing, and other transactions.
- Collaborate with Legal, Privacy, Quality, Finance, and other assurance functions on integrated compliance solutions.
- Assess emerging compliance risks, develop mitigation strategies, and provide oversight to executive leadership and governance bodies.
Requirements
- Bachelor’s degree in Law, Business, Compliance, Finance, Healthcare Administration, or a related field.
- 10–12+ years of progressive experience in healthcare compliance, legal, risk management, audit, or related fields.
- Strong knowledge of healthcare compliance laws, regulations, and enforcement practices.
- Experience influencing senior leaders and supporting compliant decision-making in highly regulated environments.
- Strong analytical, communication, judgment, decision-making, and problem-solving skills.
- Fluency in English required.
Nice to have
- Advanced degree or professional certification in compliance, legal, risk, or ethics.
- Experience in medical devices, pharmaceuticals, or the broader life sciences industry.
- Experience in highly matrixed, multicultural organizations.
- Compliance, legal, or ethics certifications.
- Change management and influencing experience.
Culture & Benefits
- Inclusive work environment centered on individual dignity, diversity, and merit.
- Global collaboration across R&D, Clinical Operations, Medical Affairs, Business Development, and assurance functions.
- Planned separation of the Orthopaedics business into DePuy Synthes may result in employment transferring to DePuy Synthes after completion of the transaction.
- Hybrid work arrangement with international travel responsibilities.
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