Trial Vendor Senior Manager

Das ist der Job

And when we do brilliant work, we can achieve remarkable things for patients as we positively transform healthcare.

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We are currently looking for a Trial Vendor Senior Manager to join our team.

Job Description As a Core member of the Clinical Trial Team (CTT) you will independently manage all vendor-related aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards, and be accountable for vendor service delivery at study level and collaborate closely with the VSM for selected services (central labs, electronic clinical outcomes assessment/electronic patient reported outcomes (eCOA/ePRO), interactive response technology (IRT), cardiac and respiratory diagnostics, patient recruitment and retention (PR&R), and imaging reading) during study start-up and leverage your technical and study start-up (SSU) expertise to ensure a timely study start-up.

Key Responsibilities Collaborate closely with the study team lead and members throughout the study lifecycle. Strong knowledge of Good Practice (GxP) and International Council for Harmonization (ICH) regulations, clinical trial design, and supplier service specifications.

Demonstrated networking abilities, team collaboration, and decision-making capabilities.

Commitment to Diversity and Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. #J-18808-Ljbffr LOCATION: Homeworking UK or Ireland or Hybrid Working at Westworks London or Dublin: Please apply only if any of these locations are accessible to you, as relocation support is not available.

ROLE TYPE: Homeworking, #LI-Home or Hybrid working, #LI-Hybrid When we put our heads together, we can do brilliant work. The main purpose of this position is to be accountable for all vendor related operational trial deliverables, according to timelines, budget, operational procedures, quality/compliance and performance standards.

To collaborate with the Vendor Start-up Manager (VSM) for the VSM’s category specific responsibilities and be responsible for all activities for which no VSM is assigned with, and for all of the service deliveries after Study Start-up when the VSM is no longer assigned to the study.

You will proactively manage vendor-related risks and potential issues and implement global vendor strategy. Drive or support the development and completion of Study Specification Worksheet (SSW) to facilitate vendor bid processes. Manage vendor interfaces in cooperation with partner functions, including quote reviews and contract negotiations.

Oversee vendor cost control, budget reviews, invoice reconciliation, and purchase order (PO) close-out. Ensure vendor service excellence at the study level, meeting quality and service standards. Optimize study start-up processes and manage central vendor-related activities (e.g., site activation, supply tracking).

Monitor vendor risk and performance using tools such as FIRST, Unified Vendor Portal (UVP), and Clinical Insights, implementing corrective actions as needed. Qualifications Bachelor’s degree or equivalent; advanced degree preferred. Fluency in English (oral and written).

Minimum of 3 years’ experience in clinical operations and vendor management processes. Proficiency in vendor management, contracting, and site-related collaborations, including Information Technology Service Management (UAT) for eCOA and IRT systems. Results-driven with proven ability to complete projects within timelines.

Excellent interpersonal, negotiation, problem-solving, and communication skills in a matrixed environment.