Lead development and generation of relevant reports and dashboards, proposing additional pertinent analyses to deliver accurate and reliable data insights to business teams, BPO network and GRA leadership
Lead analytics support in the development of key performance indicators (KPIs) and metrics for Global Regulatory Operations (GRO) and GRA
Lead projects related to transversal data management, data compliance, and analytics projects
Manage timelines and ensure goals are accomplished per agreed charter and quality standards for assigned projects
Partner with stakeholders and identify interactions or synergies with other projects/operations
Provide input to and support development of data strategy and roadmaps aligned to Sanofi business objectives and corporate Digital/ITS strategy
Serve as analytic lead contact for assigned GRA transversal activities and keep GRO/GSM&DO colleagues informed and engaged
Lead the Power BI Community of Practice, promote Power BI use, define best practices, and serve as GRA SME on Power BI
Support best practice sharing related to data processes across GRA business groups
Mentor junior staff and manage contractors as needed
Requirements
10-15 years of experience in pharmaceutical industry (listed as "10-15 years" in posting)
Strong understanding of the regulatory environment, processes, and regulations
Strong analytical, synthesis, and visual communication skills with a data mindset
Demonstrated experience in analytics (development of complex measures involving various data sources)
Demonstrated business knowledge expertise and leadership experience to work independently and direct complex projects
Ability to independently manage negotiation and business stakeholder communications and expectations
Strong interpersonal and communication skills (writing and verbal)
Proven track record of effective time management skills
Ability to think strategically and set clear direction and goals
Expertise in Excel, SQL, VBA and analytical tools (e.g., Tableau, Power BI)
Advanced programming skills in R, SAS, or Python (a plus)
Experience with a Regulatory Information System (Veeva Vault RIM preferred)
Bachelor’s or Master’s degree in Pharmaceutical or Life Sciences, Engineering, Management, Computer Science/Information Technology, or related discipline or relevant work experience
Fluent in English, both spoken and written
Competency in another language would be an added advantage
Benefits
Equal opportunities regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity
#LI-Hybrid (hybrid work indication)
Dynamic and inclusive workplace operating on trust and respect
Opportunities for career growth and development ("We are constantly moving and growing, making sure our people grow with us.")
ATS Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
analyticsdata managementdata compliancekey performance indicatorsExcelSQLVBATableauPower BIR