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Associate Director, Trial Clinical Delivery 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.

 

Your role:

We are seeking a highly skilled and strategic Project Manager to join our Global Clinical Operations team as a core member of the Clinical Trial Team (CTT). In this role, you will represent the Clinical Delivery & Patient Centricity (CDPC) team within the operational function, ensuring the successful execution of patient-centric global clinical trials. You will be responsible for enhancing site and patient engagement, optimizing site performance, overseeing vendor collaboration, implementing risk-based monitoring, identifying trends, and driving innovative operational strategies to ensure trial success.

 

Who you are:

  • Hands-on, resourceful, and strategic clinical operations professional with 8–10 years of global project management experience in clinical trials
  • Thrive in fast-paced environments, taking ownership of complex challenges and driving practical, results-oriented solutions to ensure the high-quality execution of Phase I–IIIb clinical studies
  • Present deep understanding of clinical development, site management, and regulatory requirements (ICH GCP, regional/local regulations) to enable leading with both strategic vision and operational excellence
  • Proven experience in global clinical operations, delivering high-quality trials within pharma, biotech, or CRO environments, with hands-on expertise in site management, study planning, and execution.
  • Therapeutic area expertise in Oncology, Neurology, and/or Immunology is highly desirable.
  • Resourceful problem solver with a proactive, solution-focused mindset, capable of identifying risks early and implementing practical strategies to keep studies on track.
  • Strong leadership and interpersonal skills, including adaptability, critical thinking, communication, business acumen, and cultural awareness, allowing you to effectively influence and collaborate with diverse teams.
  • Ability to work independently while maintaining a hands-on approach, managing multiple priorities, and driving operational efficiencies to ensure on-time, high-quality study delivery.Expert knowledge of clinical development (principles and concepts as well as regulatory environment e.g., ICH GCP and applicable regional/local regulations

 

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 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!

 

Job Requisition ID:  282562
Location:  Warszawa
Career Level:  E - Professional (10+ years)
Working time model:  Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

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