Clinical Trial Support: Manage clinical trial projects locally in Germany to ensure their smooth progress. Clinical Trial Supervision and Training: Train and supervise the conduct of clinical investigations in accordance with the international clinical trial management standard ICH-GCP (International Conference on Harmonisation - Good Clinical Practice), ensuring all clinical studies adhere to the highest ethical and compliance standards. Cross-Departmental Collaboration: Collaborate closely with cross-departmental teams such as clinical, quality assurance, regulatory affairs, and project management to ensure all trial-related work is executed in line with predetermined plans and standards. Data Analysis and Reporting: Participate in the collection, collation, and analysis of trial data; provide timely reports and suggestions to relevant teams to help optimize the design and execution of clinical trials. Customer and On-Site Support: Provide technical support and training to clinical trial sites, ensuring clinical staff are proficient in equipment usage and operational procedures. Market Research and Trend Analysis: Monitor and analyze the latest technologies and market dynamics in the field to support the company’s product improvement and new product development.

Language Proficiency: Fluent in English , with the ability to communicate efficiently with teams and clients from diverse linguistic backgrounds. Proficiency in Hindi is preferred. Academic Background: Hold a degree in audiology or related biomedical fields, with experience in clinical support work. Clinical Experience: At least 3 years of work experience in clinical research or medical device fields, with practical experience in clinical research execution and equipment debugging. Technical Competence: Familiar with clinical trial operational processes and relevant regulations; proficient in using common technical tools and software in clinical research; and knowledgeable about clinical trial data management and analysis methods.