Novartis Posted September 21, 2026

Vendor Operations Lead - Global Clinical Operations (GCO)

London (The Westworks), United Kingdom FULL_TIME
Notify me about similar jobs

Novartis is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

#LI-HybridLocation: London, United KingdomRelocation Support: This role is based in London, United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.Novartis operates a Hybrid working arrangement with an expectation of 12 days per month onsite. Home Worker/Remote contracts can be considered for candidates meeting eligibility criteria. This can be discussed at interview stage if applicable.Strong vendor Quality and Compliance are critical to successful clinical development and inspection readiness. As Vendor Operations Lead - Global Clinical Operations (GCO), you will lead and strengthen the processes that prepare our vendor organization for regulatory inspections and audits. You will provide subject-matter expertise across inspection readiness, audit support, corrective and preventive actions, vendor compliance, and quality improvement, while helping colleagues respond effectively in demanding regulatory environments. Working across global functions and external partnerships, you will use compliance insights and performance trends to identify risks, improve processes, and ensure vendor activities meet Novartis standards and regulatory expectations.

Key ResponsibilitiesDrive the development and implementation of vendor operations standards, processes, and governance frameworks.Lead inspection readiness and support regulatory inspection activities across vendor partnerships and operations.Ensure consistent implementation of vendor risk assessment, selection, and compliance processes.Oversee vendor quality and compliance metrics, identifying trends, risks, and improvement opportunities.Develop and maintain templates, tools, and operational resources supporting vendor governance and compliance.Support audit planning, preparation, and follow-up, including corrective and preventive action management.Act as a subject-matter expert on vendor compliance, inspection readiness, and quality management practices.Partner with global and local stakeholders to strengthen operational consistency and regulatory compliance.Drive continuous improvement initiatives that enhance vendor performance, quality outcomes, and inspection readiness.Deliver training and communications supporting adoption of systems, processes, and compliance requirements.Essential RequirementsUniversity degree in business or a relevant field, or equivalent professional experience.Typically 8-10+ years’ experience in clinical operations, including systems, regulatory requirements, and third-party/vendor management.Strong knowledge of Good Clinical Practice and regulations (GCP, GxP and ICH).Demonstrated experience supporting and leading regulatory inspections and managing inspection back-room activities.Experience with inspection readiness, storyboards, evidence collection, and regulatory document request management.Experience supporting corporate or supplier audits and developing and managing corrective and preventive actions.Strong understanding of clinical trial design, vendor compliance, and third-party requirements across clinical operations.Proven global matrix leadership, including independent ownership, analytical decision-making, and diplomatic stakeholder influence. 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: £ 67,900.00 - 126,100.00 GBP Annual   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:   https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf   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 / EEONovartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve. You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards 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.

Job details

Seniority
Not listed
Function
Clinical Development
Therapeutic area
Not listed
Location
London (The Westworks), United Kingdom
Employment type
FULL_TIME

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 858 comparable Clinical Development roles across 105 biopharma companies.

858Comparable roles tracked
811Currently active
105Companies hiring similar roles
35Countries represented

Salary context

306 of 858 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject $67,900/yr – $126,100/yr
Peer group range $0 – $458,800 (median $232,625)

Where these roles are based

Top locations among the 858 comparable roles

United States461
India119
United Kingdom50
Japan29
Spain26
Poland25

+ 29 more countries

Seniority mix

701 of 858 peers have a known seniority level

Director192
Manager163
Senior102
Associate Director102
Senior Director38
Executive/VP29
Intern/Fellow/Postdoc27
Associate24
Principal24

Therapeutic area mix

157 of 858 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology95
Immunology20
Neuroscience16
Cardiovascular / CVRM6
Ophthalmology5
Respiratory5
Dermatology & Aesthetics5
Rare Disease3
Vaccines & Infectious Disease1
Gastroenterology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Amgen Limited Uxbridge, United Kingdom Manager
Same function Same country
40%similar
BMS Business Services Ltd Uxbridge, United Kingdom Associate Director
Same function Same country
40%similar
Mylan Pharma UK Limited Sandwich, United Kingdom Principal
Same function Same country
40%similar
Regeneron UK Limited Uxbridge1, United Kingdom Associate Director
Same function Same country
40%similar
UCB Slough, Berkshire, United Kingdom
Same function Same country
40%similar
Gilead Sciences, Inc. Uxbridge, United Kingdom Senior Director
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Supplier Governance Manager
Amgen Limited · Uxbridge, United Kingdom · Manager
Function Therapeutic area Seniority Country
40%
Associate Director, Precision Medicine (Clinical Diagnostics)
Regeneron UK Limited · Uxbridge1, United Kingdom · Associate Director
Function Therapeutic area Seniority Country
40%
Clinical Trial Study Manager (1 Year FTC)
Roche · Welwyn, Hertfordshire, United Kingdom · Manager
Function Therapeutic area Seniority Country
40%
Clinical Supply Chain Forecast Manager
Ipsen Biopharm Ltd · London (UK), United Kingdom · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.