Contract

Audit Manager

Contract Assurance Reviews

Deadline 10/14/26
Sanofi

Sanofi

10,001+ employees

Global pharma company; vaccines and R&D

Compensation Overview

$105k - $151.7k/yr

Cambridge, MA, USA + 1 more

More locations: Morristown, NJ, USA

In Person

International travel of up to 20% is required, typically in 1–2 week periods.

Bachelor's, MBA

Category
Accounting (1)
Required Skills
Power BI
Microsoft Office
ERP
SAP Products
Financial analysis
Word/Pages/Docs
Tableau
Data Analysis
Excel/Numbers/Sheets
PowerPoint/Keynote/Slides

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Requirements
  • A bachelor's degree is required, preferably in Accounting, Finance, or another business discipline.
  • At least 3 years of experience in internal or external audit, forensic auditing, contract compliance, or finance is required.
  • Strong analytical and critical thinking skills with attention to detail are required.
  • Fluency in English with excellent written and verbal communication skills is required.
  • The candidate must be comfortable working across cultures and time zones in a matrixed, global environment.
  • Proficiency in Microsoft Office, including Excel, PowerPoint, and Word, is required.
  • The candidate must be willing to travel internationally up to 20%, typically for one- to two-week periods.
Responsibilities
  • Participate in planning and executing supplier audits focused on contract compliance, performance, and financial integrity.
  • Analyze supplier and company documentation to detect risks, discrepancies, or missed value.
  • Prepare clear, well-supported audit findings and quantify financial and operational impacts.
  • Engage with internal stakeholders, including Procurement, Legal, Finance, and Business Units, and with external suppliers to validate findings and support resolution.
  • Progressively lead selected audit assignments, managing scope, timelines, and stakeholder communications.
  • Track implementation of corrective actions and follow up on outcomes.
  • Contribute to supplier targeting using a risk-based approach informed by spend, contract content, performance indicators, and data trends.
  • Identify and recommend improvements to contract wording or internal monitoring practices to enhance enforceability, value realization, and risk control.
  • Help integrate audit learnings into source-to-pay and supplier relationship management activities.
  • Participate in cross-functional projects to enhance audit tools, processes, and methodologies, including Power BI dashboards, artificial intelligence pilots, and audit playbooks.
  • Contribute to continuous improvement by testing new solutions and documenting best practices.
  • Support the development of internal templates, training materials, and knowledge-sharing tools.
  • Build collaborative relationships with global teams and supplier representatives.
  • Support audit debriefs and presentations to internal audiences, helping translate findings into actionable improvements.
  • Reinforce supplier accountability and better contract execution through insights and engagement.
Desired Qualifications
  • Experience with a Big Four firm or similar consulting environment.
  • A background in healthcare and/or the life-science industry.
  • Familiarity with contract language and legal/financial terminology.
  • Experience developing written reports and delivering presentations.
  • Global or international experience and the ability to work with a diverse team.
  • Multilingual verbal and written ability.
  • Exposure to artificial-intelligence-driven audit or data-automation tools.
  • An MBA.

Sanofi is a global pharmaceutical and biotechnology company that develops, manufactures, and sells prescription medicines, over-the-counter products, and vaccines. Its products span immunology, oncology, rare diseases, and vaccines, addressing unmet medical needs through a strong focus on research and development. Sanofi's core product model relies on large-scale R&D, strategic partnerships, and licensing to bring new therapies to markets, with revenue generated from product sales and collaborations. The company differentiates itself by leveraging its global reach, diverse portfolio, and emphasis on patient-centric solutions, safety, and quality to navigate regulatory environments in developed and emerging markets. The company’s goal is to improve health outcomes and quality of life for people worldwide by delivering innovative treatments and vaccines that meet unmet medical needs.

Company Size

10,001+

Company Stage

IPO

Headquarters

Paris, France

Founded

1973

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Simplify Jobs

Simplify's Take

What believers are saying

  • Q1 2026 sales rose 13.6%, while launches grew 49.6% and Dupixent 30.8%.
  • July 2026 FDA approval expanded Sarclisa across all U.S. myeloma indications.
  • Paulo Fontoura assumed R&D leadership on September 1, 2026, accelerating pipeline execution.

What critics are saying

  • Tolebrutinib’s FDA rejection on December 24, 2025 exposed severe liver-injury risk.
  • Dupixent lawsuits consolidated in New Jersey by June 2026 threaten label and damages exposure.
  • Sanofi’s insulin plant needed €400 million German aid on September 8, 2026, signaling supply fragility.

What makes Sanofi unique

  • Dupixent posted €4.17 billion Q1 2026 sales, dominating immunology globally.
  • Sanofi’s July 2026 Sarclisa Escena became the first cancer on-body injector treatment.
  • Sanofi secured Cenrifki EU approval in June 2026, advancing a differentiated MS franchise.

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Benefits

Health Insurance

Professional Development Budget

Parental Leave

Company News

La Croix
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EU approves $448M German subsidy to Sanofi for insulin production security

The European Commission has approved a €400 million subsidy from Germany to pharmaceutical company Sanofi to maintain its Frankfurt insulin production site. The Commission stated that without this aid, Sanofi would close the German facility, reducing insulin supply security across the European Economic Area. The subsidy aims to compensate Sanofi for costs related to a service of general economic interest, strengthening insulin supply resilience for German patients. In return, Sanofi must build a new insulin factory in Frankfurt by 31 December 2032 and guarantee minimum annual production of 1.1 tonnes until 2042. Sanofi is among the world's leading insulin producers. The company announced in 2024 a €1.3 billion investment in Frankfurt to construct a new complex replacing existing facilities.

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Atlanta-based Altesa BioSciences has won the 2026 Georgia Life Sciences Golden Helix Award for Deal of the Year, recognising its oversubscribed $75 million Series B financing round. The funding, led by Forbion with participation from Sanofi, Medicxi, Pitango, and Atlantic Partners, will advance the clinical-stage pharmaceutical company's lead therapy, vapendavir. Vapendavir is an investigational oral treatment for chronic lung diseases including COPD and asthma. The drug is currently being evaluated in the Phase 2b CARDINAL trial, which will enrol 900 COPD patients across the US and UK. The Georgia Research Alliance Venture Fund was an early investor in Altesa. The company's scientific founders previously helped develop molnupiravir, one of the earliest COVID-19 treatments.

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InduPro has closed a $77 million Series B financing round and dosed its first patient in a Phase 1 study of IDP-001, its lead oncology programme. The biotechnology company is developing IDP-001, a bispecific antibody-drug conjugate targeting EGFR and a novel tumour-associated proximity antigen, for treating advanced squamous non-small cell lung cancer and other solid tumours. The Column Group led the financing round, with participation from Vida Ventures, MRL Ventures Fund, Emerson Collective, Euclidean Capital, Solasta Ventures, Sanofi, and Eli Lilly and Company. Proceeds will support Phase 1 clinical development and early proof-of-concept data generation for IDP-001, whilst advancing InduPro's broader preclinical pipeline. InduPro uses a proximity-guided platform to map protein spatial relationships on cell surfaces for discovering selective co-target pairs.

FinancialContent
Jul 24th, 2026
Scribe Therapeutics prices upsized $129M IPO at top of range

Scribe Therapeutics, a clinical-stage biotechnology company developing in vivo CRISPR technologies, has priced its upsized initial public offering at $15.00 per share, the high end of its range. The company is offering 8,580,000 shares, expecting to raise $128.7 million in gross proceeds before fees and expenses. Scribe has also granted underwriters a 30-day option to purchase up to 1,287,000 additional shares. The shares are expected to begin trading on the Nasdaq Global Market on 24 July 2026 under the ticker symbol "SCTX", with the offering closing on 27 July 2026. Additionally, Scribe has agreed to sell 500,000 shares at the same price to Sanofi in a concurrent private placement. Leerink Partners, Goldman Sachs, Guggenheim Securities, and Wells Fargo Securities are serving as joint book-running managers.