Sommario
About the Role
Major accountabilities:
- With guidance, ensures good data quality of RIM System (s) by monitoring data accuracy and completeness.
- Proactively follows up with relevant people (e.g. COs, RA CMC, HQ RA Managers) to make certain the data is updated and maintained in RIM system (s).
- Collaborates with the RIM team for implementation of new cleaning rules, and corresponding training material
- Support a compliance and quality culture within RA through effective team work and open communication
- Escalate potential compliance risks as necessary to management as appropriate
- Support implementation of RA systems in collaboration with subject matter experts and IT
- Compile regulatory compliance monitoring reports and follow ups on quality issue.
- Manage deviations/incidents/Quality Events/CAPAs in the appropriate system together with RA groups according to timelines
- Support or lead the preparation of RA for internal global audits as assigned
Key performance indicators:
- Fully compliant portfolio with internal and external regulations and procedures -Adherence to Novartis policy and guidelines -Stakeholder/ project feedback
Minimum Requirements:
Work Experience:
- Cross Cultural Experience.
- Operations Management and Execution.
- Collaborating across boundaries.
Skills:
- Scientific degree in life sciences or equivalent
- At least 2-3 years professional experience in Regulatory in Pharma or related area
- Strong knowledge of Microsoft Office Suite of applications (excel, power point, share point, OneNote, MS teams, etc.)
- Basic knowledge of the Drug Development Process and regulatory compliance for marketed products and investigational trials
- Capable to quickly learn and understand how to use RA systems
- Good interpersonal and communication skills, both oral and written
- Good analytical skills, ability to produce meaningful reports from RA systems
- Precise and independent working style with a high sense of responsibility and initiative
- Logical and methodical, with attention to details
Languages :
- English.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
Accessibility and accommodation
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
