Sant Cugat del Vallès (Barcelona)
Empresa: GRIFOLS
Requisitos: Who you are To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions). You have a Life Sciences Degree and/or Master. You speak a high level of English (C1). You have at least 5 years of experience in clinical trials. You have a knowledge of ICH GCPs, FDA CFRs, regulatory requirements and understanding of continuous change in the regulatory environment. You are familiar with Clinical Operations processes, systems and SOPs from the project management point of view. You like to communicate with your colleagues and the other departments, and you feel comfortable in environments where flexibility and dynamism is required. You pay attention to detail and prioritize competing tasks to meet deadlines to assure completion of compliance activities.
Jornada: Completa
Contrato: Indefinido