Senior Disclosure Specialist, Clinical Trials
hace 1 semana
About the Role
We are seeking a highly skilled Senior Disclosure Specialist to join our Clinical Trials team. This is an exciting opportunity to drive quality and compliance in protocol registrations and results postings.
Key Responsibilities:
- Stay Current with Global Policies & Regulations: The ideal candidate will have extensive knowledge of global policies and regulations related to clinical trials. They will be responsible for staying up-to-date with the latest developments and ensuring harmonization of Novartis transparency processes and standards.
- Represent Novartis to Internal Stakeholders: As a Senior Disclosure Specialist, you will independently represent Novartis to internal stakeholders, developing and maintaining effective working relationships with global and country multidisciplinary leaders.
- Maintain Standard Operating Procedures: You will participate in the maintenance of Standard Operating Procedures and preparations for external & internal audits, applying a continuous improvement mindset to ensure best practices are shared continually.
Essential Requirements:
- Bachelor's Degree in a Scientific Discipline: A bachelor's degree in a scientific discipline is preferred, along with minimum 3 years of pharmaceutical industry experience with knowledge in disclosure, including registration, maintenance, and results disclosure.
- Experience in Clinical Trials: Experience in clinical trials, including writing protocols, and knowledge of drug development, multiple clinical indications, and/or therapy areas is desired.
- Proven Development Skills: Proven development skills in a responsible position within Clinical Research & Development, Data Management, Project Management, Medical Writing, Regulatory Affairs or related areas are required.
Why Novartis?
At Novartis, our purpose is to reimagine medicine to improve and extend people's lives. We believe that our associates are key to achieving this goal. If you are a motivated and experienced professional looking to drive quality and compliance in clinical trials, we encourage you to apply for this exciting opportunity.
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