Senior, Clinical Trial Lead (all genders)

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.

This role can be done in a hybrid working model, 3 days from the office in Warsaw.

Your role:

You’ll lead the end‑to‑end delivery of global clinical trials for our company, guiding a cross‑functional team to hit quality, timeline, and budget targets. You’ll own study strategy, risk management, and governance, ensuring compliance with GCP and regulatory standards. From study startup to final report, you’ll coordinate with Clinical Operations, Data Management, Biostatistics, Medical, Regulatory, Safety, Supply Chain, and vendors to keep plans sharp and decisions clear. Expect 30% travel domestically/internationally; on-site position; you’ll lead Ph I-IV studies and drive continuous improvement in project management. You’ll thrive in a fast‑paced setting, deliver outcomes, and manage a study team.

Who you are:

• Advanced degree (MPH/MS/MA/MBA/PharmD) with 6+ years in clinical research and 5+ years in clinical trial management across Phase I–IV, including Phase III/registrational work.
• Strong expertise in ICH‑GCP, quality systems, inspection readiness, and CAPA delivery for global trials.
• Proven project management and ability to lead in ambiguous, fast‑paced environments with cross‑functional teams.
• Excellent collaboration and stakeholder management across Clinical Development, Operations, Regulatory, Safety, Biostats, Medical Writing, and vendors.
• Oncology experience or broad therapeutic exposure; familiarity with RBM/CTMS tools and risk management.
• Clear, impactful communicator with high emotional intelligence, resilience, and a track record of delivering on time and within budget.

YOUR MAIN BENEFITS:

• Health and well-being: Get access to private medical care, life insurance, and sports card, receive prepaid lunch card  
• Work-Life balance: Enjoy additional paid days off, flexible working hours.
• Learning and Development: Take advantage of co-financing for language courses, trainings, and certifications as well as other development opportunities
• Employee support and engagement: Benefit from Employee Assistance Program and join employee engagement groups for support and connection.

 Information on how we process your personal data for recruitment purposes, you can find on the registration form in our Recruitment Portal.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity!