Experteer Overview
Join Novartis to lead how we disclose clinical research, ensuring transparent, accurate communication aligned with general 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 reporting

Responsabilidades
• Bachelor in Life Sciences
• Previous experience in clinical trial disclosure, including work related to study conduct and data analysis
• 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 stakeholders

Requisitos principales
• flexible 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