Associate Clinical Study Manager

Summary

Location : Hyderabad, India

Step into a role where your expertise drives innovation in clinical research. As an Associate Clinical Study Manager, you'll play a pivotal part in shaping the future of patient care by ensuring our studies are executed with precision, quality, and compassion. At Novartis, your contributions will directly impact lives, and you'll be empowered to grow in a collaborative, purpose-driven environment.

About The Role

Key Responsibilities

• Maintain and update Clinical Trial Management Systems (CTMS) and Trial Master File (TMF), and related platforms to ensure accuracy and compliance.
• Assist in planning, tracking, and reporting clinical study budgets accurately
• Monitor study progress, escalate issues, and coordinate with Study Leads and External Service Providers.
• Support meeting logistics, documentation, and reporting for clinical teams.
• Take ownership of delegated tasks and champion process improvements.

Essential Requirements

Desirable Requirements

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

Skills Required

Budget Tracking, Good Clinical Practice, Financial Forecasting