艾彼達健康科技顧問股份有限公司

AIBEDA is a Contract Research Organisation (CRO) specialising in medtech and AI-powered healthtech innovation. The company provides end-to-end services, including regulatory strategy, clinical protocol design, technology assessment, and market entry support, to help clients navigate the global regulatory landscape. With a focus on agility, data-driven insights, and global connectivity, AIBEDA transforms complex regulatory challenges into commercial success. Are you passionate about clinical research? Are you excited about medtech breakthroughs impacting people’s health? If the answers are yes, we want to hear from you.

AIBEDA is a Contract Research Organisation (CRO) specialising in medtech and AI-powered healthtech innovation. The company provides end-to-end services, including regulatory strategy, clinical protocol design, technology assessment, and market entry support, to help clients navigate the global regulatory landscape. With a focus on agility, data-driven insights, and global connectivity, AIBEDA transforms complex regulatory challenges into commercial success. Are you passionate about clinical research and project management? Are you excited about medtech breakthroughs impacting people’s health? If the answers are yes, we want to hear from you.

【Company Description】 AIBEDA is a Contract Research Organisation (CRO) specialising in medtech and AI-powered healthtech innovation. The company provides end-to-end services, including regulatory strategy, clinical protocol design, technology assessment, and market entry support, to help clients navigate the global regulatory landscape. With a focus on agility, data-driven insights, and global connectivity, AIBEDA transforms complex regulatory challenges into commercial success. 【Role Description】 This is a full-time on-site role based in Taipei. The Business Development Manager is responsible for identifying new business opportunities, building and managing client relationships, and contributing to strategic growth initiatives. In addition to traditional business development activities, the role involves engaging with innovative medtech and healthtech clients to understand their commercial, clinical, and regulatory needs, often collaborating with internal experts to co-develop tailored solutions that support early-stage development, market access, and product success.

AIBEDA is a Contract Research Organisation (CRO) specialising in medtech and AI-powered healthtech innovation. The company provides end-to-end services, including regulatory strategy, clinical protocol design, technology assessment, and market entry support, to help clients navigate the global regulatory landscape. With a focus on agility, data-driven insights, and global connectivity, AIBEDA transforms complex regulatory challenges into commercial success. We are seeking an experienced Clinical Data Manager & Biostatistician to join our team. This dual-role position will oversee all aspects of clinical data management and perform statistical analyses to support the design, execution, and reporting of clinical trials. The ideal candidate will ensure high-quality, compliant data capture and deliver rigorous statistical outputs that inform regulatory submissions and strategic decision-making.

艾彼達是一家專注於醫療科技與人工智慧驅動健康科技創新之合同研究組織（CRO）。 公司提供端對端服務，包括監管策略擬定、臨床方案設計、技術評估與市場準入支援，協助客戶暢行無阻地應對全球監管環境。 艾彼達誠徵兩名細心且負責的臨床研究協調員／研究護理師，協助臨床試驗機構的試驗流程，確保受託臨床試驗依照規範執行並產出高品質數據。

【Company Description】 AIBEDA is a Contract Research Organisation (CRO) specialising in medtech and AI-powered healthtech innovation. The company provides end-to-end services, including regulatory strategy, clinical protocol design, technology assessment, and market entry support, to help clients navigate the global regulatory landscape. With a focus on agility, data-driven insights, and global connectivity, AIBEDA transforms complex regulatory challenges into commercial success. 【Role Description】 This is a full-time hybrid role based in Taipei. The Regulatory Affairs Manager is responsible for leading regulatory strategy and submissions for medical devices in Taiwan (TFDA), the United States (FDA), and other Asia-Pacific markets. In addition to traditional regulatory responsibilities, the role plays a critical part in shaping product and clinical development strategies, particularly for innovative technologies such as AI-driven devices and software as a medical device (SaMD). By providing early-stage regulatory input, the role contributes to protocol design, clinical feasibility, and product refinement, ensuring alignment with both regulatory standards and commercial objectives.