Senior Clinical Study Manager – Global Medical Affairs

Key Responsibilities

• Lead cross-functional study teams and lead study execution operations from concept to reporting.
• Oversee study documentation, systems, and vendor/Third Party activities activities and deliverables.
• Track progress, manage budgets, risks, and ensure timely reporting and disclosures.
• Drive process improvements and operational excellence.
• Ensure compliance with process standards for quality and systems, ensure audit readiness.
• Mentor junior team members and contribute to training initiatives.

Qualifications

• Bachelor’s degree or higher in Life Sciences or Healthcare.
• 6+ years in clinical operations or project management (pharma/CRO).
• Strong knowledge of GCP and global clinical development.
• Proven leadership in matrixed environments.
• Excellent communication, strategic thinking, and stakeholder engagement skills.
• Fluent in English.

Commitment to Diversity & Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

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

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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