AstraZeneca | Germany | 22xxx, 21xxx, 20xxx Hamburg | Permanent position | Full time | Published since: 04.09.2026 on stepstone.de
Local Study Associate Director (LSAD) / Clinical Project Lead (m/f/d)
Innovative, dynamic and sustainable: As one of the world's leading companies in the research medicine industry, AstraZeneca offers the best opportunities for your personal and professional development. For we are certain that research is the foundation of our future. We at AstraZeneca focus on science. It encourages us to constantly expand the limits of the potential and create new things. We believe in the power of ideas and drive them forward to fundamentally improve the treatment of diseases. With passion we work every day to improve the lives of people through science. In our Site Management & Monitoring area, the clinical trials take a decisive step towards developing our innovative medicines to make them available as quickly and extensively as possible as modern therapy options for patients. Our study teams work in a challenging and complex environment where excellent teamwork and competent specialists are equally important. .
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Your tasks • Your profile • What we offer
If you now think “Here is my future!” we look forward to your application as Local Study Associate Director (LSAD) / Clinical Project Lead (m/w/d), Office-based. You can also find a workplace with excellent perspectives where you can fully exploit your potential. Influence: Project management of global and local clinical studies Conducting studies according to the latest Good Clinical Practice guidelines, legal requirements and global and local standard operating procedures with appropriate time, budget, resource and quality requirements Responsibility for Feasibility tests, selection of the test physician:inside and determination of the patient:internal recruitment targets Budget planning, monitoring and control, incl. Completion of corresponding internal and external contracts Budget responsibility for project accounts and ongoing review of staff resources at study level
Strengths prove: Complete university studies: Ideally in biology, health sciences, medicine, pharmacy, public health or a related area. Multiannual experience and knowledge in the field of clinical research: experience in CVRM and/or R&I with corresponding studies of designs in multicentric, Phase II/III studies in Germany. Understanding regulatory requirements and operations. Embossed communication capability, safe occurrence, moderation of cross-functional meetings; management of a study or project team; Monitors of CRA activities Detection and handling of operational and scientific risks, independently initiates solutions and escalations, drives decisions and ensures implementation up to the result. First experience with Feasibility and SiteEngagement, as well as in budget/cost control (honoring) and contract management with test centers. English language skills. Readiness to travel: Flexible visits to test centres in Germany and participation, as well as to supra-regional meetings/trainings.
It offers: an attractive pipeline and innovative products individual development opportunities and the focus on lifelong learning lots of trust, appreciation and space for co-design in a focused and passionate team a diverse, inclusive and prejudice-free working environment committed to the Charter of Diversity and not only allows differences, but actively promotes a sustainable company that becomes CO2 negative by 2030 along the entire value chain an attractive benefit package such as EGYM Wellpass, Corporate Benefits and much more
Do you want to become part of our mission and increase the quality of life of numerous patients? Then apply now. .
Location
![]() | AstraZeneca | |
| Hamburg | ||
| Germany |
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