Associate Clinical Study Manager at Novartis

Hyderabad, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

01 Feb, 26

Salary

0.0

Posted On

03 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trials, Conflict Management, Contract Management, Effective Communication, Financial Analysis, Negotiation Skills

Industry

Pharmaceutical Manufacturing

Description

Job Description Summary #LI-Hybrid 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. Job Description 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 Bachelor’s degree or higher in life sciences or equivalent education and experience Minimum 3 years of clinical operations or project management experience Strong knowledge of Good Clinical Practice and global clinical development processes Proven ability to work independently and escalate issues appropriately Experience in planning, executing, and reporting clinical studies Fluent in English (oral and written) Desirable Requirements Experience in financial forecasting, cost reconciliation, and budget tracking Skills Desired Clinical Trials, Conflict Management, Contract Management, Effective Communication, Financial Analysis, Negotiation Skills Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

Responsibilities

The Associate Clinical Study Manager will maintain and update Clinical Trial Management Systems and ensure compliance. They will monitor study progress, escalate issues, and coordinate with Study Leads and External Service Providers.