Asset Management Compliance Specialist

hace 24 horas


Vigo, España OPIS A tiempo completo

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis. Although professional experience and qualifications are key for this role, please ensure you have the preferred interpersonal skills before applying if required. The Regulatory Submissions Specialist contributes to the management and development of procedures related to the activities in which he/she is involved and ensures that the outputs of their activities meet the quality standards required by the company. Develops and maintains knowledge of global and local regulatory requirements and industry practice/guidelines for submission activities to local requirements. Manages contract and budget negotiation/execution with sites/investigators/other parties involved as applicable. Responsibilities Develop and maintain knowledge of global and local regulatory requirements and industry practice/guidelines for submission activities. Manage contract and budget negotiation/execution with sites, investigators, and other parties as applicable. Qualifications Fluent in English. Good planning, problem solving, and organizational skills. About OPIS OPIS is an International CRO with 25 years of experience in conducting Phase I‑IV, non‑interventional and medical devices studies on an international level. We always offer state‑of‑the‑art information technology solutions and innovative approaches to the increasing complexity and variety of projects. OPIS’s extensive expertise covers all phases of drug‑related trials, taking care of the Sponsor beyond the therapeutic area, and also offering accurate clinical investigations for medical and diagnostic devices. With Global Clinical Research Locations all over the world, OPIS offers a full range of integrated clinical research services as scientific advice, medical writing, trial start‑up, monitoring, study management, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture as well as quality assurance and training. #J-18808-Ljbffr



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