Responsible for the development, execution and reporting of clinical trials in support of the registration of a product
Development of abbreviated protocol and clinical protocol
Participation in the review process for protocols, study reports, labeling, and interactions with regulatory agencies and ethics committees
Drive breakthroughs that could turn the impossible into possible for millions
Ensure that all development activities are targeted towards timely achievement
Interact with opinion leaders and external consultants
Serve as medical monitor for the studies assigned
Ensure clinical data meets all necessary regulatory standards

Medical Doctor with transplant, nephrology, hepatology or immunology clinical expertise preferred
Minimum 2 years experience in pharmaceutical drug development and/or clinical research
Proven record of scientific achievement as evidenced by presentations and publications in peer-reviewed journals and/or successful completion of major clinical studies or submissions is a plus
Strong scientific and academic background with deep understanding of the disease
Clinical research or pharmaceutical experience medicine experience in transplant/immunology field
Knowledge of drug development and in immunology
Good networking ability in cross-cultural environment
Strong interpersonal, communication, presentation, and negotiation skills across all levels of the organization
Performance oriented with ability to work along agreed timelines and a focus on strategy and execution
Fluent in English (verbal and written communication).

Clinical Research Director – Immunology and Inflammation

Key skills