Sanofi Pasteur Inc.

Sanofi Pasteur Inc.

Portfolio Strategy Associate VIE Contract

Morristown, NJ · Full-time

Sponsorship not specifiedDetected 8 days ago
SparkExcelSupply ChainLogisticsClinical TrialsFDA RegulatoryCommunicationTime ManagementPublic SpeakingAdaptabilityMicrosoft OfficeSharePointRegulatory Affairs

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odds of building a lasting career here

40Risky
Cap-exempt (no lottery)0
Sponsors this role90
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

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Employer immigration record

from this employer's Department of Labor filings

Green-card filing pattern in this occupation

Context, not a finding about this posting: of this employer's 5 green-card filings in this occupation, 100% were for a worker who already held the job.

Files H-1B transfers

3 transfer filings in the last year, covering 3 workers. Median labor-condition decision: 7 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

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About the role

  • Therefore, only applications that are submitted in English will be considered.
  • Please make sure to apply with your personal email address.
  • About the job As Portfolio Strategy Associate VIE within Global Regulatory Portfolio Strategy & Innovation team, you'll play a key role in supporting the evolution of our Blueprint model.

Responsibilities

  • Support the deployment and continuous improvement of the GRA Blueprint Model across US-based regulatory teams, ensuring consistent adoption and effective use.
  • Support GRA project risk management capability building by coordinating training sessions and providing user support for the R&D project risk management tool.
  • Support the end-to-end PRS (Probability of Regulatory Success) process implementation, including data collection, analysis, and reporting.
  • Support testing cycles and user acceptance activities for regulatory digital tools.
  • Maintain documentation repositories and ensure information is accessible and up-to-date.
  • GRA Blueprint Model Support & Enhancement

Nice to have

  • At least 1-year full time experience working in the pharmaceutical /biotechnology industry.
  • Experience with project coordination or cross-functional team collaboration.
  • Exposure to regulatory affairs, drug development, or related R&D functions is a plus.

Skills

  • Proficient with Microsoft Office 365 suite (Word, Excel, PowerPoint, Teams).
  • Familiarity with SharePoint and collaborative digital platforms.
  • Interest in AI/digital tools and regulatory data platforms.
  • Strong analytical skills with attention to detail and data accuracy.
  • Ability to quickly learn new software tools and systems.
  • Excellent organizational and time management skills with ability to handle multiple priorities.
  • Strong written and verbal communication skills, with ability to synthesize complex information.
  • Proactive, self-motivated, and able to work autonomously in a matrixed environment.
  • Adaptable and comfortable with ambiguity in a fast-paced, changing environment.
  • Intellectual curiosity and eagerness to learn about regulatory strategy and drug development.
  • Master's degree in Life Sciences, Pharmacy, Regulatory Affairs, or related scientific discipline.
  • Fluent English (verbal and written).

Benefits

  • Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.
  • Sanofi unites people who are passionate about solving healthcare needs across the world.

Company info

  • At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
  • Be part of a pioneering biopharma company where patient insights shape drug development.

Visa & Work Authorization

  • is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship
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This listing is sourced directly from Sanofi Pasteur Inc.'s careers page and normalized into a canonical job model.