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Sr Project Manager

hace 2 semanas


Madrid, España Avania A tiempo completo

Avania are hiring - Senior Project Manager - Medical Devices  As the Sr Project Manager, you will have the opportunity to provide leadership through planning, organizing and overseeing all clinical trial activities and deliverables from study start-up to close out. The Senior Project Manager is responsible for the scope, schedule, budget and quality of multi site, multi service complex clinical trials involving; implementing and managing the project planning; tracking of the clinical monitoring process; administration and overview of clinical trials. The position requires a proactive approach in developing the project planning and monitoring of both resources and clinical trial so that all aspects of the plan can progress effectively. The Sr Project Manager will: Supervise the Project Team to ensure trial deliverables are on time, within budget and in appropriate quality, in compliance with applicable SOPs, ISO14155 / ICH-GCP and all applicable (local) regulations  Manage the project planning and tracking of trial progress of various international clinical trials from start-up to close out The role of Sr Project Manager also has financial responsibilities, and you will: Maintain and perform regular budget reviews for your allocated studies Assist the Management Team in preparing budgets and forecasts as required and possibly have involvement in bid defense meetings Since Quality is in our DNA, a key responsibility of the Senior Project Manager role is to keep our quality standards high for our clients Candidates who offer a combination of the skills, knowledge and experience listed below are encouraged to apply to Avania's Senior Project Manager role. With our continued growth we are hiring talent to join us on our journey and grow with us. We ask Relevant degree in (para)medical life science or nursing preferred. GCP-ICH-E6, FDA regulations and ISO 14155,13485 and 9001 knowledge where applicable  Knowledge of regulatory regulations and guidelines on medical devices Prior PM experience of multi site, multi service complex clinical trials with a strong finance/budget management skill set Experience within  Medical Device/MedTech with a focus on cardiovascular therapeutics  7+ years' experience in clinical trials with at least 1 year as a Sr. CRA preferred Ability to travel domestically and internationally Proficient in the use of computer and software systems (Microsoft Word, Excel, PowerPoint, email) Fluent in spoken and written English, with excellent communications and interpersonal skills We offer The opportunity to work in an innovative, fast-growing and rewarding industry A dynamic and enthusiastic global team that fosters collaboration and the opportunity to work with experts across many specialties Exchange of knowledge and ideas to help employees grow and advance their careers, backed with training and other development opportunities Competitive compensation and benefits package (details shared during the interview process) Some roles offer the opportunities for travel Ask us about our hybrid and fully remote work opportunities We look forward to receiving your application When you need to advance your career, it takes Avania  #LI-DNI