Summary

• The Clinical Sourcing Manager generates, negotiates and complete contracts to support the utilization of clinical Contract Research Organizations (CROs) for Novartis Clinical Trials. Assuring the business of a compliant, high quality, timely and efficient external service delivery to support the Novartis drug development pipeline. The Clinical Sourcing Manager also participates in projects

About the Role

Position Title : Clinical Sourcing Manager - Medical Affairs

Location - Hyderabad #LI Hybrid

About the role :

• Initiatives to ensure Clinical Contracting & Outsourcing Management is prepared to successfully respond to the changing needs and requirements (legal, operational, regulatory, and financial) of our customers.
• Prepare and release RFI, RFP and RFQs and negotiate with existing and new suppliers to support business for new requests as well as re-negotiating scope changes.

• Act as the main point of contact with vendors for negotiation of the scope of work, study assumptions, pricing, and payment schedules.
• Ensure agreements are commercial advantageous to Novartis while minimizing risk through close collaboration with functional partners such as legal, finance, and QA.
• Ensure ESP selection is based on current category strategy, valuable services, cost avoidance and savings opportunities. Delivering a robust implementation to improve value and drive spend/contract compliance - to also include ongoing monitoring and reduction of maverick spend
• Drive annual efficiency improvements in applicable spend categories and responsible for complete contract packages for clinical ESP activities. Secure all necessary approvals to ensure compliance to SOX and company procedures.
• Chip in to vendor audit requests and facilitate corrective action plans. Ensure ESPs are delivering in line with expectations and contracts.

• IMPACT - Chips in to specific projects for a category of spend and implementing the global service and category strategy. Financial impact in terms of savings generation Detailed understanding of the clinical development process and robust understanding of the management of clinical trials.
• Excellent influencing and negotiating skills. Solid understanding of contractual legal terms and conditions and hands on to Clinical CRO marketplace including central laboratories, reference laboratories and specialty providers
• Solid financial understanding as it relates to clinical trial contracts and cost elements. analyzing specifications for optimization. Linking specification to customer value, challenging specification confidently. Conveying messages clearly and convincing partners. Able to identify proactively and pursue new insights and opportunities, acting as an innovation agent and modifying approach and behaviors as vital to create customer value.
• Planning, organizing and leading projects taking into account priorities, resources, budgets, issues and constraints to achieve desired results; defining clear project scope and objectives; applying software and tools to plan, track and report status.
• Achieving results by proactively building long-term, sustainable and effective relationships, understanding the partner landscape and demonstrating political astuteness across business structures and networks.
• Key skills required: Understanding or Hands-on experience in contracting/ budgets/ forecast /procurement knowledge etc. - 40% Customer management & communication - 50% Flexibility to un/learn, negotiations & team player - 10% and Clinical trial knowledge is a plus

• Master's Degree/other advanced degree in the area of science, business or related field is preferred; an MBA in addition would be an advantage (Lifesciences/Chemistry / Biochemistry or Pharmaceutical sciences is required).
• Solid understanding of the Comparators market with minimum of 9 years' experience in Clinical Development / Pharma R&D / Procurement and outsourcing within the Pharma or CRO industry.