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Externally Sponsored Research Manager

7+ years
USD 100,500.00 - 167,500.00
10 Oct. 27, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

🧪 Job Title: Externally Sponsored Research Manager

📍 Location: Cambridge, Massachusetts | Morristown, New Jersey
🏢 Type: Regular | Onsite
📅 Posted On: October 9, 2025
⏳ Closing On: December 31, 2025
💰 Salary Range: USD 100,500 – 167,500


🌍 About the Company

Sanofi is a global healthcare leader dedicated to transforming the lives of people with immune challenges, rare diseases, cancers, blood, and neurological disorders. Our teams—from R&D to sales—collaborate worldwide to revolutionize treatment, improve patient outcomes, and connect communities.
We chase the miracles of science every day to make a real impact on millions of lives.


💼 About the Role

The Externally Sponsored Research (ESR) Manager oversees and manages the operational aspects of unsolicited research support requests, including Investigator Sponsored Studies (ISS) and Externally Sponsored Collaborations (ESC).
This role ensures all proposals are scientifically reviewed, compliant, and efficiently executed from submission to study closeout.

You will report to the Senior Manager, ESR Operations, and collaborate across medical, regulatory, supply chain, and compliance teams.


🎯 Key Responsibilities

  • Manage ESR studies from proposal submission to closeout, including contracting, payments, product supply, and performance tracking.

  • Ensure compliance with Sanofi SOPs, local laws, and global regulations (GCP, ICH, OIG, PhRMA).

  • Support Scientific Review Committee (SRC) processes — concept, protocol, and amendment reviews.

  • Maintain ESR system of record, ensuring data integrity, audit readiness, and reporting accuracy.

  • Collaborate cross-functionally for timely agreements, supply forecasts, and performance metrics.

  • Provide information for CMO reporting and other global initiatives.

  • Train internal stakeholders on ESR tools and systems.

  • Support communication of safety updates and Dear Investigator Letters (DILs).


🎓 Qualifications

Education:

  • Minimum Bachelor’s degree (Life Sciences or related field preferred).

Experience:

  • At least 3 years of relevant experience in a medical or regulated pharmaceutical environment.

  • Strong project management skills (certification preferred).

  • Familiarity with Investigator Sponsored Studies and regulatory standards (GCP, ICH, PhRMA Code).

  • Excellent analytical, communication, and cross-functional collaboration skills.

  • Proven ability to improve efficiency and manage complex workflows.


💡 Core Competencies

Competency

Description

Stretch

Challenge the status quo, focus on high-impact priorities, and strive for excellence.

Take Action

Act decisively, take informed risks, and move projects forward proactively.

Act for Change

Embrace innovation and evolve ESR Operations for greater effectiveness.

Cooperate Transversally

Build strong collaboration across teams to improve program execution.

Strategic Thinking

Drive timely, informed decisions aligned with long-term goals.

Develop People

Commit to personal growth and empower others.

Commit to Customers

Understand and exceed internal/external stakeholder expectations.


💎 Why Join Sanofi?

  • Bring the miracles of science to life with a passionate, future-ready team.

  • Explore global career growth through promotions, cross-functional or international moves.

  • Enjoy a comprehensive rewards package recognizing your performance.

  • Access health, wellness, and prevention programs for you and your family.

  • Benefit from at least 14 weeks of gender-neutral parental leave.


⚖️ Equal Opportunity Statement

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action Employers.
All qualified applicants will receive consideration without regard to race, color, creed, religion, national origin, age, sex, gender identity/expression, sexual orientation, disability, veteran status, or any other protected characteristic.


🚀 Join Us

At Sanofi, your growth can be as transformative as the work we do.
Together, we’ll push boundaries, challenge convention, and build smarter solutions for patients worldwide.

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