Trial Vendor Associate Director

Das ist der Job

Eligibility criteria apply and can be discussed at interview, if applicable.

Darum lohnt es sich

Key Responsibilities • Act as the single point of contact for vendor service delivery at the study level, partnering with vendors and cross-functional teams within the Clinical Trial Team (CTT) • Provide end-to-end oversight of vendor deliverables, ensuring alignment with study timelines, scope, and quality expectations for vendors including (but not limited to) eCOA, central labs, IRT, cardiac, PR&R • Review vendor-related protocol sections during protocol development.

Work with the Vendor Start-up Manager to ensure that the protocol is appropriately represented in the vendor specifications • Oversee vendor financials, including budget tracking, invoice reconciliation, and PO management and close-out • In collaboration with vendors, study start up leads and vendor start up managers, ensure that all key vendor deliverables and documentation are in place to support submission during study start-up • Lead UAT activities for vendor systems (e.g., eCOA, IRT), and contribute to vendor system validation • Drive site activation from a vendor perspective, compile vendor related central documents, and address risks/issues during site activation and throughout the life-cycle of a site • Manage vendor performance, risks, and issue resolution, driving mitigation plans in collaboration with vendors and study teams Essential Requirements • Significant industry experience with clinical operations and vendor management processes (ideally 5+ years). • Strong understanding of GxP and ICH regulations. • Solid knowledge of clinical trial design and alignment to supplier requirements. • Experience conducting User Acceptance Testing (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.

Preferable Requirements • Audit & inspection experience • Sponsor/CRO/vendor acquisition or transition studies experience • Protocol writing experience Benefits & Rewards At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.

The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs.

Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable.

Commitment to Diversity and Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverseteams’representative of the patients and communities we serve.

Salary Range £67,900.00 - £126,100.00 Expected Annual Base Salary Range for role £67,900.00 - £126,100.00 Annual Job Description Summary #Hybrid The location for this role is Westworks, London, UK.

The preferred working arrangement is Hybrid with an expectation of 12 days per month onsite, however this role can also be offered on a Remote working basis for people based in the UK only. This position is also available in Dublin, Ireland, on a Hybrid working basis only. Please apply to the specific Dublin requirement for this location.

Novartis cannot support relocation for these positions. Please apply only if these locations are accessible to you. Novartis cannot sponsor Visas for these locations. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.

In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. You may be eligible for a company vehicle or a car allowance in accordance with the applicable local Novartis policies and guidelines.

Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.

A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

Skills Desired Budget Management, Clinical Trials, Contract Management, Process Improvements, Project Planning, Vendor Management