Experteer Overview Envíe su solicitud a continuación después de leer todos los detalles y la información de apoyo sobre esta oportunidad de trabajo. Join Novartis to lead how we disclose clinical research, ensuring transparent, accurate communication aligned with global rules. You will guide cross-functional teams—clinical, medical, statistical, and legal—to deliver high-quality disclosures that build trust and support scientific progress. This role blends regulatory stewardship with strategic process improvement in a fast-moving environment. You’ll shape disclosure planning, stay ahead of evolving regulations, and foster a culture of transparency and quality. This opportunity offers meaningful impact on public understanding of clinical research.Compensaciones / Beneficios• Assess study eligibility and manage registration, maintenance, and results disclosure across public clinical trial registries• Ensure all study data, including protocols and clinical study reports, are accurately represented in public databases• Oversee timely updates to study records to meet global regulatory and organizational requirements• Collaborate with clinical, medical, statistical,



and legal partners to align on disclosure expectations and deliverables• Provide expert guidance to study teams on registry requirements and disclosure processes• Lead routine trainings to strengthen internal understanding of Clinical Disclosure Office processes• Support process improvements by contributing to updates of Standard Operating Procedures and training materials• Monitor evolving global regulations and incorporate changes into disclosure planning and execution• Partner with cross-functional teams to resolve data discrepancies or compliance risks related to disclosure• Champion a culture of transparency and quality by promoting best practices in clinical registry reportingResponsabilidades• Bachelor in Life Sciences• Previous experience in clinical trial disclosure, including work related to study conduct and data analysis xcskxlj • Strong knowledge of global legislation, regulations, and guidelines governing clinical trial transparency• Solid understanding of Good Clinical Practice regulations and how they apply to study disclosure activities• Ability to adapt to evolving needs, contribute ideas, and constructively challenge established processes• Proven capability in building effective working relationships with internal and external stakeholdersRequisitos principales• adaptable and hybrid working options• minimum 14 weeks paid parental leave• insurance plans• retirement plans• wellbeing resources• global recognition programs

📌 Senior Manager, Clinical Disclosure Office (Barcelona)
🏢 Novartis
📍 Barcelona