Researcher, Image Analysis and Artificial Intelligence Leader

The Global Clinical Program Lead (GCPL) is a key member of the Global Project Team, leading the Strategic Clinical Team within Global Clinical Development. The role involves collaboration across various departments such as R&D, Regulatory, Patient Safety, Medical Affairs, and more. The GCPL is responsible for ongoing benefit-risk evaluations of clinical assets, providing leadership in clinical development strategy, and overseeing the implementation of clinical plans for assigned projects. This position mainly focuses on early or late-stage development projects but may involve tasks across different stages. It requires strong analytical, synthesis, and communication skills, with a high degree of autonomy. Tasks & Responsibilities Define clinical development strategies, milestones, and resource needs in collaboration with cross-functional teams. Plan and execute Phase 2 and 3 studies, including dose-finding and pivotal studies for regulatory approval. Provide clinical/medical leadership within internal and external teams for assigned assets. Represent Global Clinical Development in meetings and serve as the primary contact for Medical Affairs, Market Access, and Marketing. Guide Clinical Study Teams to align trial conduct with overall strategy. Design, deliver, and interpret clinical study results ensuring ethical and scientific integrity in compliance with GCP. Review and approve key clinical trial documents. Review ongoing study data and perform benefit-risk evaluations. Ensure peer review of study and program designs. Analyze and present clinical trial results to internal/external committees. Oversee clinical content of study documents and regulatory submissions. Lead scientific meetings and advisory boards with experts and key opinion leaders. Represent the company in meetings with Health Authorities and external stakeholders. Support study-specific committees and oversee external diligence processes. Lead and chair Strategic Clinical Teams. Education & Experience Medical degree; dermatology specialty is a plus. Advanced degree (PhD or Master’s in Pharmaceutical Medicine) is valuable. Experience in clinical research, preferably in Dermatology or Immunology. Minimum of 3 years in pharmaceutical drug development. Understanding of clinical research methodologies. Hands-on experience in drug development with scientific credibility. Fluency in English; proficiency in MS Office. Strong data analysis, communication, and presentation skills. Leadership and collaboration skills, strategic mindset, and problem-solving abilities. Values Care: Emphasizes listening, empathy, valuing diversity, and mutual success. Courage: Challenges the status quo, takes ownership, and learns from experiences. Innovation: Focuses on patient-centered solutions, creativity, and entrepreneurial spirit. Simplicity: Acts decisively, understands reasons behind actions, and maintains agility and clarity. J-18808-Ljbffr

Location: torrejón-de-ardoz, ES

Posted Date: 5/15/2025