Job Description

Summary

As a tactical BOM, you will participate in proactively supporting tactical budget activities across the Biomedical Research Translational Medicine (BR-TM) organization. The role strengthens op-erational budget consistency, improves financial risk detection, and ensures high-quality budget execution across budget life cycle early development related to TM deliverables.

This role complements the end-to-end budget management and oversight under the Portfolio Resources and Finance Management group. Whilst not having any direct overall clinical budget responsibility the BOM needs to have a solid understanding of budget activities and forecasting. It is also of huge benefit that the TBM is familiar with basic clinical study/early development conduct terms and timings.

About The Role

Major Accountabilities

  • Proactively provide tactical solutions for daily budget tasks during study conduct and other cross-TM cost activities. Serve as first contact for basic budget support and PO and invoice matters from study maintenance onward.
  • Oversee and monitor PO activity and budget impact. Detect risks and communicate to Clinical Finance Manager. Deliver quarterly PO risk assessments on GR IR balances.
  • Track budget impact from contracts and amendments. Support timely, current budget planning and forecasting.
  • Ensure tracking systems and data sources are accurate and up to date.
  • Support Therapeutic Area-level budget deliverables. Provide Clinical Finance Managers with PO-related financial risk inputs.
  • Support end-of-trial budget activities. Partner with Clinical study team and drive timely, accurate PO closeouts.
  • Identify budget risks and opportunities. Communicate and report to relevant stakeholders
  • Contribute to process improvement.
  • Support internal TM processes with guidance on requirements and best practices.
  • Represent your function to deliver tactical support to Translational Management. Collect data and track KPIs and other performance indicators.
  • Liaise with customers and partners to align actions and track deliverables.
  • Maintain supporting IT systems to keep information accurate.

Education (minimum/desirable)

Undergraduate degree, preferably in a scientific discipline or life science background or equivalent work experience

Languages

Fluent English (oral and written)

Experience/Professional Requirement

  • Minimum 5 years’ experience in Clinical Operations (early development), procurement or trial budget execution.
  • Total experience of 10+ years, Understanding of clinical study processes and milestones.
  • Strong communication and stakeholder management.
  • Proactive problem solver.
  • Ability to navigate financial systems and maintain data accuracy.
  • Ability to prioritize work, multi task, manage time appropriately in a fast paced/high volume environment.
  • Proven cGCP background

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

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.

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Job Details

Role Level: Mid-Level Work Type: Full-Time
Country: India City: Greater Hyderabad Area
Company Website: http://www.novartis.com/in-en Job Function: Manufacturing & Production
Company Industry/
Sector:
Pharmaceutical Manufacturing

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About the Company

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