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Clinical Sourcing Manager, R&D
Novartis
Selangor
Sur place
MYR 80 000 - 100 000
Plein temps
Il y a 16 jours

Résumé du poste

A leading pharmaceutical company is seeking a Clinical Sourcing Manager to oversee the negotiation and execution of contracts with Contract Research Organisations (CROs) for clinical trials. This role requires a strong background in Clinical Development and Outsourcing, alongside excellent negotiation skills. Join us in advancing the drug development pipeline and making a meaningful impact in patients' lives.

Qualifications

  • Minimum 5 years’ experience in Clinical Development.
  • Minimum 5 years’ experience in Outsourcing within Pharma or CRO.
  • Strong negotiation skills for managing contracts.

Responsabilités

  • Negotiate and execute contracts with CROs.
  • Ensure compliance and quality in service delivery.
  • Collaborate with legal and finance teams for risk management.

Connaissances

Clinical Development
Contract Negotiation
Vendor Management
Budget Development

Formation

Bachelor’s degree in Life Sciences or Pharmaceutical Sciences
Master’s/advanced degree or MBA
Description du poste
Overview

Job Title: Clinical Sourcing Manager, R&D

Location: Hyderabad, India

The Clinical Sourcing Manager generates, negotiates, and executes contracts to support the utilisation of clinical Contract Research Organisations (CROs) for Novartis Clinical Trials. This role assures compliant, high-quality, timely, and cost-effective external service delivery to support the Novartis drug development pipeline. The Clinical Sourcing Manager also participates in projects and initiatives to ensure Clinical Contracting & Outsourcing Management is prepared to respond to changing needs and requirements (legal, operational, regulatory, and financial).

Major accountabilities
  • Prepare and release RFI, RFP, and RFQs; negotiate with suppliers for new requests and scope changes.
  • Act as the main contact with vendors for negotiation of scope of work, study assumptions, pricing, and payment schedules.
  • Negotiate, develop, and execute contract frameworks (including MSAs & SLAs) with key suppliers and ensure implementation.
  • Collaborate with legal, finance, and QA to ensure agreements are commercially advantageous and minimise risk.
  • Select ESPs based on category strategy, value-added services, cost avoidance, and savings opportunities.
  • Drive productivity improvements and ensure spend/contract compliance, including monitoring and reduction of maverick spend.
  • Ensure complete contract packages for clinical ESP activities and secure necessary approvals for compliance.
  • Contribute to vendor audit requests and facilitate corrective action plans.
  • Ensure ESPs deliver in line with expectations and contracts.
  • Proactively identify and pursue new ideas and opportunities to create value.
Minimum Requirements
  • Work Experience:
    • Minimum Bachelor’s degree in Life Sciences or Pharmaceutical Sciences required.
    • Master’s/other advanced degree or MBA in business administration or a scientific field preferred.
    • Minimum 5 years’ experience in Clinical Development, including clinical trial budget development.
    • Minimum 5 years’ experience in Outsourcing within Pharma or CRO industry.
Languages
  • English.
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?

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

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