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Transversal Study Information Operations Manager

Sanofi
Sanofi
10 years
preferred by company
10 Jan. 15, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Transversal Study Information Operations Manager

Locations: Swiftwater, Pennsylvania | Multiple Global Locations
Employment Type: Full-Time | Permanent
Function: Study Information Management / Clinical Operations
Experience Level: Senior / Leadership
Experience Required: Minimum 10 years in pharmaceutical study operations, regulatory reporting, and project management
Salary Range: USD 148,500 – 214,500 (commensurate with experience)


Job Overview

Sanofi is seeking a highly skilled Transversal Study Information Operations Manager to oversee global operational strategies for the collection, tracking, and internal communication of clinical study information. This role ensures Sanofi meets international, regional, and local obligations for clinical data and regulatory reporting. The position collaborates with cross-functional teams in Medical, PV/Safety, Real-World Evidence (RWE), Quality, Digital, and reporting groups, ensuring timely, accurate, and compliant study information delivery.


Key Responsibilities

Data Governance & Management

  • Maintain governance for clinical study information across multiple data sources and Sanofi tracking systems

  • Ensure internal stakeholders have access to complete, accurate, and up-to-date study documentation for regulatory and non-regulatory requests (e.g., DSUR, PBRER, NDA Annual Reports)

  • Collaborate with operational teams to enforce data quality, consistency, and completeness within tracking systems and document repositories

  • Track and communicate performance and compliance metrics to support business needs

Stakeholder Collaboration

  • Develop and maintain relationships with key internal stakeholders, including PSPV, GRA, Medical and Clinical Trial Disclosure teams, Global Business Units (GBUs), HEOR/HEVA teams, pharmacoepidemiology, market access, and managed access program teams

  • Coordinate actions and communication across multiple functional entities

  • Support Real-World Evidence processes in partnership with Sanofi Business Operations

Operational Excellence

  • Lead transversal coordination of study information across global and regional teams

  • Ensure standardized processes for data collection, reporting, and communication across clinical operations

  • Implement process improvements and drive proactive solutions for study information management


Required Qualifications

Education:

  • Bachelor’s Degree from an accredited university (life sciences, scientific, digital, or related background preferred)

Experience:

  • Minimum 10 years of combined experience in study management, regulatory/safety reporting, project management, and pharmaceutical operations

  • Proven experience in matrixed, global environments managing cross-functional initiatives

Technical Skills:

  • Proficiency with clinical data tracking systems, databases, and information management tools

  • Strong understanding of data flow, governance, and reporting processes

  • Knowledge of business intelligence tools such as Power BI is an advantage

  • Fluent in English (written and spoken)

Professional Competencies:

  • Customer- and quality-focused with high attention to detail

  • Strong project management and transversal coordination capabilities

  • Excellent communication, networking, and stakeholder management skills

  • Ability to work collaboratively in global teams and demonstrate proactivity and urgency


Why Join Sanofi

  • Be part of a global, innovation-driven biopharmaceutical company shaping the future of healthcare

  • Opportunity to lead strategic initiatives across clinical operations, regulatory, and real-world evidence programs

  • Access career growth, international exposure, and leadership development opportunities

  • Competitive rewards and benefits, including healthcare, wellness programs, and gender-neutral parental leave


Equal Opportunity Statement

Sanofi is committed to diversity, equity, and inclusion. Employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, sex, gender identity, sexual orientation, age, disability, veteran status, or other characteristics protected by law.


Apply now on thepharmadaily.com to lead global study information operations and help Sanofi deliver innovative therapies that improve patient outcomes worldwide.