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Clinical Trial Manager

hace 3 meses


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.Clinical Trial Manager Madrid, Community of Madrid Clinical Trial ManagerMadridMadrid, Community of Madrid, ES Working with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers. Bms. Com/working-with-us. The Clinical Trial Manager will be responsible for study oversight and delivery management (time, budget, quality) at country level from start-up to closure. Responsibilities:Serves as the main point of contact at a country level for internal and external stakeholders. Coordinates country cross functional teams and acts as the main point of contact for a Country with the protocol manager and other global study team membersCoordinates with other internal roles in country and site feasibility processDevelops country level patient recruitment strategy & risk mitigation. Leads problem solving and resolution efforts including management of risk, contingencies, issue resolution and escalationAssessment and set up the of vendors during study start up periodResponsible for preparing country specific documents (e. G. global country specific amendment)Responsible for verifying and confirming with local team eTMF completenessReviews Site Monitoring visit reports, takes action within the timelines specifiedEnsures inspection readiness of assigned trials within country. Leads study team meetings locallyRequirements:Bachelor's degree required preferably within life sciences or equivalentMinimum of 4 years' industry related experienceProven experience in Project Management and leading multi functional teamsExperience in leading or participating as an active member of cross functional teams, task forces, or local and global initiativesStrong scientific backgroundThorough understanding of Country regulatory environmentIn-depth knowledge and understanding of clinical research processes, regulations and methodologyUnderstanding of clinical landscape with practical knowledge of a variety of medical settings and medical records managementDemonstrated organizational and planning skills and independent decision-making abilityAbility of critical thinking and risk analysis