Trial Vendor Associate Director

Collaborate closely with study team lead and members throughout the study lifecycle.

Review vendor-related protocol sections during protocol development.

Manage vendor interfaces and support contract negotiations in collaboration with procurement.

Oversee vendor cost control, budget reviews, invoice reconciliation, and purchase order (PO) close-out.

Ensure vendor service excellence, maintaining quality and service standards at the study level.

Drive site activation, compile central documents, and address risks/issues during site activation.

Conduct user-acceptance testing (UAT) for electronic Clinical Outcome Assessment (eCOA) and Interactive Response Technology (IRT) systems.

Monitor vendor-related cycle times and risks using tools like FIRST, while implementing corrective actions as needed.

5+ years of experience with clinical operations and vendor management processes.

Strong understanding of Good Practice (GxP) and International Council for Harmonization ICH regulations.

Solid knowledge of clinical trial design and alignment to supplier requirements.

conducting UAT for eCOA and IRT systems.

Proven expertise in vendor management, including outsourcing, contracting, and sourcing clinical services.

Results-oriented, with a track record of completing projects on time.

Ability to collaborate effectively in cross-functional teams within a matrixed environment.

Strong influencing, negotiation, communication, and problem-solving skills.

Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world.

How can we achieve this?

With our people.

It is our associates that drive us each day to reach our ambitions.