Associate Director Clinical Data Manager

hace 4 días

Barcelona, España Merck A tiempo completo

.Associate Director Clinical Data Manager (All Genders)BarcelonaBarcelona, Catalonia, ES Work Your Magic with usReady to explore, break barriers, and discover more? We know you've got big plans – so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. A great opportunity has opened within the Data Monitoring, Management and Innovation department to further strengthen our Clinical Data Management team. As an Associate Director Clinical Data Manager, you will play a crucial role in managing and overseeing clinical data management activities within the organization. You will be responsible for ensuring the integrity, accuracy, and completeness of clinical trial data, while also coordinating a team of clinical data management professionals in a matrix setting. Your role: Accountable for all Clinical Data Management (CDM) related deliverables in assigned global (Phase I-IIIb) trials or programs of varying complexityProvide CDM leadership for assigned trial(s)/program(s), take global accountability and serve as the CDM representative at the study/program levelDemonstrate project management and operational expertise in the strategic planning and delivery of CDM deliverables at study/program level, e. G.Planning timelines and resources, risk identification and management, status tracking, internal and external stakeholder management etcDefine and execute risk-based data collection, cleaning and quality assurance strategies for eCRF and external data (including coding)Ensure the accuracy, integrity, and completeness of clinical trial data through comprehensive data review and validation activitiesEnsure quality of clinical database/deliverables (incl. eCRF and external data) as well as submission readiness of the clinical data management deliverables and data packages (e. G. CDISC)Act as primary point of contact within CDM for any HA submission related activities (e. G

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