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Portfolio Strategy Associate VIE

Job in Morristown, Morris County, New Jersey, 07960, USA
Listing for: Sanofi
Full Time, Contract position
Listed on 2026-08-30
Job specializations:
  • Business
    Business Analyst
Salary/Wage Range or Industry Benchmark: 65000 - 90000 USD Yearly USD 65000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: Portfolio Strategy Associate VIE Contract

Portfolio Strategy Associate - VIE Contract

Location:

United States of America, Morristown

Target start date: 01/01/2027

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28. PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship. PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide.

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. Blueprint is GRA’s approach to developing regulatory strategies with the ambition to achieve ONE Regulatory voice and deliver well-differentiated, value-added, sustainable products with competitive product labels. In this role, you will support the development, maintenance, and deployment of the Blueprint framework, helping to strengthen our operating model, simplify ways of working, and ensure alignment across processes, governance, templates, and roles & responsibilities.

You will work closely with key stakeholders across GRA, gaining exposure to global regulatory strategy, organizational design, and transformation at scale.

Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.

Main responsibilities

GRA Blueprint Model Support & Enhancement Support the deployment and continuous improvement of the GRA Blueprint Model across US-based regulatory teams, ensuring consistent adoption and effective use. Contribute to Blueprint model evolution by gathering user feedback, documenting lessons learned, and identifying opportunities for optimization. Assist in the development and delivery of Blueprint training materials and onboarding programs for new users.

Project Risk Management & PRS Implementation Support GRA project risk management capability building by coordinating training sessions and providing user support for the R&D project risk management tool. Assist in quality control of risk data migration and new risk entries to ensure consistency and completeness. Support the end-to-end PRS (Probability of Regulatory Success) process implementation, including data collection, analysis, and reporting.

Contribute to transparent PRS tracking from team proposals through governance endorsement.

Digital Transformation & AI Integration Coordinate with regulatory Subject Matter Experts (SMEs) to gather requirements and feedback for TRACY (Trusted Regulatory AI Companion for You) and other digital initiatives. Support testing cycles and user acceptance activities for regulatory digital tools. Help identify opportunities for process digitalization and automation within Portfolio Strategy workflows.

Strategic Communication & Stakeholder Engagement Assist in coordinating the GRT and GRA Strategy & Innovation Forum, including logistics, content preparation, and follow-up actions. Help prepare presentations, reports, and communications for TPSC meetings and other governance forums. Maintain documentation repositories and ensure information is accessible and up-to-date.

About you Experience

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.

Soft and technical 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…

Position Requirements
10+ Years work experience
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