Associate External Operations Manager - Hyderabad (Office), India

Step into a role where your expertise will help shape the future of Medical Affairs at Novartis. As Manager Operational Excellence you will focus on process simplification performance management and governance ensuring alignment with global standards and supporting the developmen ...

This role sits at the core of driving data-driven, personalized omnichannel engagement by leading the implementation, integration and scale-up of a global Salesforce Marketing Cloud Platform. · Function as independent contributor to drive strategy through execution and deliver ca ...

The Manager - Solutions Activation and Automation supports the Associate Director in driving operational efficiency, process standardization, and automation within the US Studio Operations – Solutions Activation team. · This role manages projects, collaborates with cross-function ...

Step into a high-impact leadership role where your expertise will shape the future of global medical affairs studies at Novartis. · Lead GMA study operations for assigned therapy area from strategic planning through execution and delivery. · ...

Leads a team of Clinical Label Managers (CLM) and is accountable for operational deliverables as well as owns functional end-to-end responsibility for the team in a direct leadership role. · ...

Manages Quality aspects and projects within area of responsibility Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems Adheres to the current GxP and compliance policies of Novartis Performs designated roles such as Entity Data ...

We are hiring a Senior Specialist in our Information Security Team as part of the Data, Digital & IT function at Novartis. · As part of this role, you will oversee security operations, service line, · technology governance and interface externally and internally in accordance wit ...

The Clinical Document Governance Management (CDGM) is responsible for the strategy and implementation of clinical document management (CDM) systems, processes, and standards; as well as the operations of CDM services. · We are seeking a knowledgeable and experienced Clinical Docu ...

This role supports the development and maintenance of skills, knowledge and capabilities for associates through GxP qualification requirements and effective learning opportunities. · ...

The Manager – Payer MDM will lead the strategy, governance, and operational execution of the Payer Master Data Management (MDM) platform. · Lead Payer MDM strategy and ensure alignment with business priorities and stakeholder expectations. · Establish governance, standards, and b ...

To act as a trusted advisor offering in-country policy expertise and knowledge to support and educate leaders, managers and associates on all P&O topics on the moments that matter. People Partners support all divisional customer groups in country enabling the delivery of lifecycl ...

Specialist - Quality Operations · Job Description Summary · End to End Supplier Quality Management activities which includes Supplier onboarding, Routine Monitoring and Supplier Exits Job Description · Supplier Quality Management: · • Drafting of Annual Monitoring and Certificat ...

The Global Head Technology Integration & Tech Standards is accountable for the end-to-end definition development and continual improvement of the Clinical Trials Technology ecosystem. · Advanced degree in science engineering business or mathematics/statistics preferred · Strong u ...

The Senior Analyst will support the strategy, governance, and operational execution of the Payer Master Data Management (MDM) platform. · Support Payer MDM strategy and ensure alignment with business priorities and stakeholder expectations. · Assist in establishing governance, st ...

Provides Business Planning & Analysis (BPA) Finance support for the global Real Estate and Facility Services (REFS) domain. · ...

Associate Clinical Sourcing Manager · Job Description Summary · The associate clinical sourcing manager is responsible for generating, negotiating, and executing contracts to support the utilisation of clinical Contract Research Organisations (CROs) for Novartis Clinical Trials. ...

Step into a role where your expertise drives innovation on the manufacturing floor. · ...

250 Active clinical trials are supported by Global Clinical Supply (GCS), 100k shipments are sent out annually and 1.5 million patient kits are packed. · ...

R&D Quality Manager provides quality assurance expertise to development and research organizations. They manage projects to ensure compliance with GxP regulations. · Support maintenance of regulatory-required files for health authority inspections. · Generate Quality Plans for cl ...

This is a pivotal role where your expertise in serialization and product tracking will shape the future of pharmaceutical operations. As the Global Process Owner, you'll lead the charge in optimizing end-to-end processes, driving automation and ensuring compliance across global m ...