Experteer Overview

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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 integral 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 xqbhyrx
- 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