Senior Clinical Disclosure Lead
hace 5 días
Job Description
We are seeking a highly skilled Senior Clinical Disclosure Lead to join our team at Novartis, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. This is a hybrid role that can be based in either Barcelona, Spain or London, UK.
About the Role
The Senior Clinical Disclosure Lead will ensure quality and compliant protocol registrations and results postings as well as alignment with global registries (i.e. ClinicalTrials.Gov, EudraCT, EUCTIS, Novartis Clinical Trial Results EMA-HMA Catalogue of non-interventional studies, etc.) with oversight. They will also be accountable for protocol registry and results eligibility assessment and must demonstrate capability to interpret, discuss, and ensure appropriate trial data is accurately represented in clinical registries.
Key Responsibilities:
- Participate in client trainings within Biomedical Research and Novartis Pharmaceuticals to drive quality and compliance and organizational alignment to changing disclosure requirements.
- Responsible for staying current with global policies & regulations and operational application to ensure harmonization of Novartis transparency processes and standards.
- Independently represent Novartis to internal stakeholders.
- Develop and maintain effective working relationships with global and country multidisciplinary leaders, such as Study Leads, M.D.S, Legal, and Business Development & Licensing.
- Participate in the maintenance of Standard Operating Procedures and preparations for external & internal audits.
- Apply a continuous improvement mindset ensuring best practices are shared continually driving to the most productive processes.
Essential Requirements:
- Bachelor's degree in a scientific discipline preferred.
- Minimum 3 years pharmaceutical industry experience with knowledge in disclosure including registration, maintenance, and results disclosure.
- (Experience with ClinicalTrials.Gov, EudraCT, and the Citeline Disclose tool (also known as PharmaCM) advantageous.)
- Knowledge of drug development, experience in writing protocols, experience in multiple clinical indications and/or therapy areas desired.
- Proven development skills in a responsible position within Clinical Research & Development, Data Management, Project Management, Medical Writing, Regulatory Affairs, or related areas.
- Ability to successfully work within a complex cross-divisional matrix; previous experience leading multidisciplinary teams in a matrix environment.
- Strong negotiation & conflict resolution skills; well organized, focused on results/compliance, strong planning, tracking, problem-solving, and decision-making skills.
- Proficiency in Good Clinical Practice, Regulatory Processes, and clinical trial designs.
- Ability to adapt to a changing external environment.
Why Novartis?
Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world. With a competitive estimated salary of €85,000 - €110,000 per year, we offer a unique opportunity to grow your career while making a meaningful impact. Join us in shaping the future of healthcare and discover how you can contribute to our mission.
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