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Novartis

Trial Vendor Senior Manager - Global Clinical Operations

London
£49.1k – £91.3k/yr
Posted 4 days ago
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Salary Range: £49,140.00 - £91,260.00

Job Description Summary

#LI-Hybrid
Location: Westworks, London, UK

We are unable to offer relocation for this position. Please only apply if this location is accessible for you. This is a hybrid position with an expectation of 12 days a month onsite working from our Westworks, White City, London offices.


When we put our heads together, we can do brilliant work. And when we do brilliant work, we can achieve remarkable things for patients as we positively transform healthcare.

Our Trial Vendor Senior Managers have a direct impact on the success of our clinical trials and the management of our critical vendors.


Job Description

As a core member of the Clinical Trial Team (CTT), the Trial Vendor Manager (TVM) serves as the CTT vendor sub-team lead, independently managing all vendor-related aspects of global clinical trials to deliver study outcomes in accordance with schedule, budget, quality, compliance, and performance standards.

The TVM is accountable for vendor service delivery at the study level and collaborates closely with the Vendor Start-up Manager (VSM) for selected services, including central labs, eCOA/ePRO, IRT, cardiac and respiratory diagnostics, patient recruitment and retention (PR&R), and imaging reading.

During study start-up, the TVM leverages technical and study start-up expertise to help ensure timely study initiation. You will proactively manage vendor-related risks and potential issues and implement global vendor strategy.

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

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Essential Requirements:

  • Bachelor’s degree in Life Sciences or equivalent; advanced degree preferred.
  • Minimum of 3 years’ experience in clinical operations and vendor management processes.
  • Strong knowledge of GxP and ICH regulations, clinical trial design, and supplier service specifications.
  • Proficiency in vendor management, contracting, and site-related collaborations, including 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.
  • Demonstrated networking abilities, team collaboration, and decision-making capabilities.
  • Strong scientific curiosity and good knowledge of working on Clinical Trials with an Oncology focus, would be highly beneficial

Benefits & Rewards

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.

Expected Annual Base Salary Range for role: £49,140.00 - 91,260.00

The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies, and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.

In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.

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.

In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.

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.

Read our brochure to learn more about our global total rewards offering: Novartis Life Handbook

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

Commitment to Diversity and Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.

Skills Desired

Budget Management, Clinical Operations, Clinical Process, Clinical Research Operations, Clinical Trials, Clinical Trials Operations, Clinical Trial Support, GxP Compliance, GxP Regulations, Process Improvements, Project Planning, Vendor Contract Management, Vendor Management, Vendor Quality Management, Vendor Relationship Management, Vendor Risk Management, Waterfall Model


Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you.

Working together. Learning together. Thriving together.

Discover how you can join us in changing people’s lives. Novartis Careers

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.

Novartis is aware of employment scams which make false use of our company name or leader’s names or recruiter’s names to defraud job seekers. Novartis does not make job offers without interview and never asks candidates for money. If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money, or personal information. Novartis is not responsible for any claims, losses, damages, or expenses resulting from scams.

In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov.

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Skills

Budget Management
Clinical Operations
Clinical Process
Clinical Research Operations
Clinical Trials
Clinical Trials Operations
Clinical Trial Support
GxP Compliance
GxP Regulations
Process Improvements
Project Planning
Vendor Contract Management
Vendor Management
Vendor Quality Management
Vendor Relationship Management
Vendor Risk Management

Location

London, England, United Kingdom

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