Finde einen Job 
Finde eine Ausbildung 
Top Arbeitgeber 
Top Universitäten 
Für Unternehmen Auf einen Blick
- Aufgaben: Lead global safety programs, ensuring product safety and collaborating with cross-functional teams.
- Arbeitgeber: Join a diverse team innovating in Healthcare, Life Science, and Electronics to enrich lives globally.
- Mitarbeitervorteile: Flexible work culture, personal development opportunities, and a commitment to diversity and inclusion.
- Warum dieser Job: Be part of a mission-driven team that impacts patient lives and champions human progress.
- Gewünschte Qualifikationen: MD or equivalent with 10+ years in pharma/biotech, including 5-6 years in Global Patient Safety.
- Andere Informationen: Location flexibility includes Switzerland; embrace a culture of curiosity and innovation.
Das voraussichtliche Gehalt liegt zwischen 72000 - 84000 € pro Jahr.
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That\’s why we are always looking for curious minds that see themselves imagining the unimaginable with us.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
Your Role:
We are looking for a Global Program Safety Lead who will ensure the safety of assigned products or portfolios in collaboration with the Therapeutic Area Head. This role requires innovative strategic input and scientific leadership to maintain the integrity of safety medical assessments. You will set the medical safety strategic direction and escalate significant safety signals or issues as needed.
Proactive safety signal and benefit-risk management are vital, necessitating collaboration with various R&D functions. You will contribute safety expertise to the Clinical Development Plan, ensuring it addresses safety risks effectively. High-quality representation of Global Program Safety on cross-functional teams is essential for informed project decision-making.
Your responsibilities include overseeing benefit-risk analysis in key documents like periodic safety reports and risk management plans. You will also contribute to product-related documents, including clinical trial protocols and reports. Engaging with external experts and providing medical safety expertise for due diligence activities are also part of your role.
Who You Are:
- MD or equivalent with accredited residency
- Minimum of 10 years in the pharmaceutical/biotechnology industry, including 5-6 years in Global Patient Safety (esp. in analysis & interpretation)
- Profound experience in safety monitoring and strategy during clinical drug development (pharmaceutical, biotech, CRO)
- Mastery of global regulatory requirements for drug safety and pharmacovigilance
- Exceptional data analysis skills
- Proficiency in signal detection and evaluation as well as understanding of continuous Benefit-Risk Assessment
- Strong medical judgment in safety decision-making
- Proven matrix management and project leadership experience in cross-functional teams with strong influence skills
- Excellent communication and presentation skills in English, both written and oral
We also consider Switzerland as a possible location.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!
#J-18808-Ljbffr
Global Program Safety Lead (all genders / full- or part-time) Arbeitgeber: Merck Gruppe
Kontaktperson:
Merck Gruppe HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Global Program Safety Lead (all genders / full- or part-time)
✨Tip Number 1
Familiarize yourself with the latest trends and regulations in global patient safety. Understanding the current landscape will not only help you in interviews but also demonstrate your commitment to the field.
✨Tip Number 2
Network with professionals in the pharmaceutical and biotechnology industries. Attend relevant conferences or webinars to connect with potential colleagues and learn about their experiences in safety monitoring and strategy.
✨Tip Number 3
Prepare to discuss specific case studies or examples from your past experience that highlight your expertise in benefit-risk assessment and safety signal management. This will showcase your practical knowledge during discussions.
✨Tip Number 4
Demonstrate your leadership skills by sharing instances where you've successfully influenced cross-functional teams. Highlighting your ability to lead and collaborate effectively will resonate well with the hiring team.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Global Program Safety Lead (all genders / full- or part-time)
Tipps für deine Bewerbung 🫡
Understand the Role: Take the time to thoroughly read the job description for the Global Program Safety Lead position. Understand the key responsibilities and required qualifications, as this will help you tailor your application effectively.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in the pharmaceutical or biotechnology industry, particularly in Global Patient Safety. Make sure to detail your expertise in safety monitoring, data analysis, and regulatory requirements.
Showcase Communication Skills: Since excellent communication skills are essential for this role, provide examples in your application that demonstrate your ability to communicate complex information clearly and effectively, both in writing and verbally.
Express Your Passion: Convey your enthusiasm for the healthcare field and your commitment to improving patient safety. Share any relevant projects or initiatives you've been involved in that align with the company's mission of enriching lives through science and technology.
Wie du dich auf ein Vorstellungsgespräch bei Merck Gruppe vorbereitest
✨Showcase Your Experience
Make sure to highlight your 10+ years in the pharmaceutical or biotechnology industry, especially your 5-6 years in Global Patient Safety. Be ready to discuss specific examples of how you've contributed to safety monitoring and strategy during clinical drug development.
✨Demonstrate Your Analytical Skills
Prepare to discuss your exceptional data analysis skills and how you've applied them in previous roles. Be ready to provide examples of signal detection and evaluation, as well as your approach to continuous Benefit-Risk Assessment.
✨Communicate Effectively
Since excellent communication skills are crucial for this role, practice articulating your thoughts clearly and concisely. Prepare to present complex safety information in a way that is understandable to cross-functional teams.
✨Emphasize Collaboration
Highlight your experience in matrix management and project leadership within cross-functional teams. Be prepared to discuss how you influence and collaborate with various R&D functions to ensure informed project decision-making.
