PbFrom Nature. For Health. /bDr. Willmar Schwabe is the worlds leading manufacturer of herbal medicines. As a family owned company with over 150 years of history and around 4,000 employees worldwide, we stand for products of exceptionally high quality. To promote the health of people all over the world, we rely on modern research, customer orientation and competent and motivated employees./p pbIt starts with nature. With you./b Join us to lead a clinical research project and make a difference as:/p pbClinical Project Manager (f/m/d)/b/p pbLocation:/b KarlsruhebrbCompany:/b Dr. Willmar SchwabebrbDivision:/b RDbbrStart:/b 01.07.2025brbType of employment:/b fulltime/pbrul libClinical Study Planning Execution: /bTake ownership of clinical trials in the role as sponsor and of non interventional healthcare studies in a fully outsourced model first task will be a clinical trial to prove the effectiveness of our standardized extract of Ginkgo biloba leaves in/li libStudy Start Up Compliance: /bEnsure study feasibility, regulatory compliance, and ethics approvals, contribute to the creation of study plans, documents and systems, manage project/li libVendor CRO Management: /bSelect, qualify, contract and guide external partners while applying effective sponsor oversight and quality control across all trial/li libCross functional Leadership: /bLead internal and external project teams with clarity and drive keeping timelines, budgets, and responsibilities on track through every stage of the/li libQuality Documentation Excellence: /bEnsure correct and complete documentation of the study, and train teams on study specific procedures and SOPs while patient safety, data quality and legal alignment are paramount./li /ulbrul libProfessional qualifications: /bYou hold a degree in a scientific or health care discipline, such as medicine, pharmacy, biology, biochemistry or equivalent. Alternatively, you are qualified through relevant experience./li libExperience: /bProfessional experience in clinical research project management (pharmaceutical industry or contract research organization). Experience in conducting clinical studies in APAC region especially China would be an/li libSkills and competencies: /bYou combine a profound knowledge of ICH GCP, other relevant ICH guidelines and the European laws and guidelines regarding clinical research with strong project management abilities and skills in MS/li li