YOUR OPPORTUNITY The IT SOX Senior Associate is a key contributor to the execution and continuous improvement of the Bacardi’s Sarbanes-Oxley (SOX) IT compliance program. This role leads and performs advanced-level testing of IT general controls (ITGCs),
The Associate Director, Data Products will play a critical role in accelerating the transition from legacy data and reporting capabilities to the organisations strategic data platform. The role will focus on translating business priorities into scalable data
Job Overview Associate Clinical Project Management Directors supervise, manage and provide oversight to assigned Clinical Project Management staff who manage or support studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and
Company Description Glovo is part of the Delivery Hero Group, the world’s pioneering local delivery platform, our mission is to deliver an amazing experience—fast, easy, and to your door. We operate in around 65 countries worldwide.
Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of
Scopely is looking for an Associate Product Manager to join our MONOPOLY GO! Game team in Barcelona hub on a hybrid basis (3X week in office). At Scopely, we care deeply about what we do and want
About Finom Finom is a European tech startup headquartered in Amsterdam, and we’re on a journey towards revolutionizing the financial landscape for entrepreneurs worldwide. Our mission is to develop an all-in-one financial B2B solution that integrates
About the Role We are looking for a Custom Made Device Leader / Planner. In this role, you will join a specialized team designing custom stent grafts for complex aortic aneurysms. This role blends clinical insight
Job Description Summary Job Description GE Vernova - The Energy to Change the World With over 130 years of experience and proven innovation, GE Vernova is leading a new era of energy. We are electrifying the
Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Job Overview Site monitoring and site
Description Are you a detail-oriented Business Analyst who loves turning business needs into smart, actionable solutions? Do you thrive on collaborating with cross functional teams, translating complex requirements into clear functional specifications, and seeing your ideas
Hello! Si le interesa solicitar este empleo, por favor, asegúrese de cumplir los siguientes requisitos que se enumeran a continuación. At Factorial were looking for a new Procurement Associate to help us support and scale our Finance
Overview: Desplácese hacia abajo para ver todos los requisitos del puesto y las responsabilidades que pueden esperar los candidatos seleccionados. WELCOME TO SITA At SITA, we keep airports moving, airlines flying smoothly, and borders open. Our
Senior Procurement Associate At Factorial we’re looking for a new Senior Procurement Associate to help us elevate and scale our Finance team’s procurement function. The role involves leading procurement strategy and supplier management across the company, managing Factorials
Job Overview Compruebe que cumple con los requisitos de habilidades para este puesto, así como con la experiencia asociada, y luego envíe su CV a continuación. The Associate Medical Director / Medical Director will provide medical, clinical
Experteer Overview Todos los candidatos deben asegurarse de leer atentamente la siguiente descripción del puesto y la información antes de enviar su solicitud. In this role you will advance pharmacovigilance within AstraZeneca’s oncology programs, shaping safety
Job Overview The Associate Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during
Introduction To Role This role is based in Barcelona, with an on-site commitment of three days a week. Fluency in English is required. The Associate Regulatory Affairs Director (ARAD) is an experienced regulatory specialist with strong project
Regulatory Affairs Sr Associate As part of our R&D team, you will have the opportunity to work with the Regulatory Affairs team for the Beverage business across Europe to ensure compliance with food regulations, support innovation and
Experteer Overview Inscríbase (haciendo clic en el botón correspondiente) después de revisar toda la información relacionada con el trabajo a continuación. As a core member of the Clinical Trial Team, you will own vendor operational delivery